Cardiac muscle-associated genes

ABSTRACT

The invention provides compositions and novel polynucleotides and their encoded proteins that serve as surrogate markers in that they co-express with genes known to be involved associated with disorders associated with cardiac muscle function. The invention also provides expression vectors, host cells, proteins encoded by the polynucleotides and antibodies which specifically bind the proteins. The invention also provides methods for the diagnosis, prognosis, evaluation of therapies and treatment of disorders associated with cardiac muscle function.

[0001] This application is a continuation-in-part of U.S. Ser. No. 09/299,708, filed Apr. 26, 1999.

FIELD OF THE INVENTION

[0002] The invention relates to 48 polynucleotides associated with cardiac muscle function that were identified by their coexpression with known cardiac muscle-associated genes. The invention also relates to the use of these polynucleotides, their encoded proteins and antibodies which specifically bind the proteins in diagnosis, prognosis, treatment, and evaluation of therapies for disorders associated with cardiac muscle function.

BACKGROUND OF THE INVENTION

[0003] Vertebrates have three classes of muscle: skeletal, smooth, and cardiac. Skeletal and cardiac muscles have a striped appearance in the light microscope and are therefore called striated. Cardiac muscle resembles skeletal muscle in many respects, but it is specialized for the continuous, involuntary, rhythmic contractions needed for pumping blood. Smooth muscles lack striations and surround internal organs such as the intestines, the uterus, and large blood vessels. Skeletal muscle is under the voluntary control of the nervous system. Cardiac muscle and smooth muscle are under the involuntary control of the nervous system. Compared with striated muscles, smooth muscle cells contract and relax slowly and can create and maintain tension for long periods of time.

[0004] Muscle tissue is composed of bundles of multinucleated muscle cells (myofibers). Each muscle cell contains bundles of actin and myosin filaments (myofibrils) which extend the length of the cell. The myofibril is composed of a chain of sarcomeres. The sarcomere is the functional unit of contraction. Myosin filaments are sandwiched between alternating layers of actin filaments. Myosin filaments are composed of heavy and light chain proteins. Actin filaments are capped by two proteins, capZ and tropomodulin. In addition, the myosin-binding sites of actin filaments are protected by the tropomyosin-troponin regulatory complex. Contraction of muscle is initiated by action potential-stimulated release from the sarcoplasmic reticulum of calcium ions into the cell to levels greater than 10⁻⁶ M. Binding of calcium ions to troponin causes tropomyosin to move towards the center of the actin filament. This movement exposes the myosin-binding sites of actin. Prior to contraction, the N-terminal domain of the myosin heavy chain-light chain complex (myosin head) forms a cross-bridge with actin filaments. Binding of ATP to the myosin head causes dissociation of myosin from actin. This is followed by a conformational change of the myosin head and hydrolysis of ATP. The myosin head then forms a new cross-bridge with actin filaments. Successive cycle of ATP-binding, dissociation from actin, conformational changes, ATP hydrolysis, and crossbridge formation results in muscle contraction. Relaxation is initiated when calcium ion levels in the cell fall below 10⁻⁶ M. At that level, calcium ions dissociate from troponin, which then shields the myosin-binding sites of actin.

[0005] Gap junctions, very permeable parts of the cell membrane, connect individual muscle cells with each other. Through these gap junctions, ions diffuse relatively freely and transmit action potentials to all muscle cells.

[0006] Differentiation of muscle cells during embryogenesis and ontogeny is regulated by a number of nuclear transcription factors such as myogenin, MyoD, MEF2A, and myf-5, and by cell cycle proteins such as p21, p57, and RB. Expression of the genes which encode some of these myogenic regulatory proteins has been correlated with certain type of tumor and other disorders (Wang et al. (1995) Am J Pathol 147:1799-1810; Miyagawa et al.(1998) Nat Genet 18:15-17; and Sedehizade et al.(1997) Muscle Nerve 20:186-194).

[0007] Contemporary techniques for diagnosis of cardiac muscle abnormalities rely mainly on observation of clinical symptoms, electrocardiograms, and serological analyses of metabolites and enzymes. Relatively mild symptoms in the earlier stages of heart disease may even be overlooked. In addition, the serological analyses of the limited number of hormones or peptides do not always differentiate among those diseases or syndromes which have overlapping or near-normal ranges of hormonal or marker protein levels. Thus, development of new techniques, such as microarrays and transcript imaging, will contribute to the early and accurate diagnosis or to a better understanding of molecular pathogenesis of cardiac disorders.

[0008] The present invention satisfies a need in the art by providing new compositions that are useful for diagnosis, prognosis, treatment, and evaluation of therapies for disorders associated with cardiac muscle function.

SUMMARY OF THE INVENTION

[0009] The invention provides a composition comprising a plurality of polynucleotides having the nucleic acid sequences of SEQ ID NOs:1-48 that are highly significantly co-expressed with known the cardiac muscle-associated genes: atrial regulatory myosin, ventricular myosin alkali light chain, cardiac troponin, cardiac ventricular myosin, cardiodilatin, creatine kinase M, myoglobin, natriuretic peptide precursor, sarcomeric mitochondrial creatine kinase, telethonin, titin, and urocortin.

[0010] The invention also provides an isolated polynucleotide comprising a nucleic acid sequence selected from SEQ ID NOs:1-48 and the complements thereof. In different aspects, the polynucleotide is used as a surrogate marker, as a probe, in an expression vector, and in the diagnosis, prognosis, evaluation of therapies and treatment of disorders such as atherosclerosis, arteriosclerosis, atrial fibrillation, cancer (myxoma) and complications of cancer, cardiac injury, congestive heart failure, coronary artery disease, hypertension, hypertrophic cardiomyopathy, myocardial hypertrophy, myocardial infarction, and plaque. The invention further provides a composition comprising a polynucleotide and a labeling moiety.

[0011] The invention provides a method for using a composition or a polynucleotide to screen a plurality of molecules and compounds to identify or to purify ligands which specifically bind to the composition or the polynucleotide. The molecules are selected from DNA molecules, RNA molecules, peptide nucleic acids, peptides, mimetics, ribozymes, transcription factors, enhancers, and repressors.

[0012] The invention provides a method for using a composition or a polynucleotide to detect gene expression in a sample by hybridizing the composition or polynucleotide to nucleic acids of the sample under conditions for formation of one or more hybridization complexes and detecting hybridization complex formation, wherein complex formation indicates gene expression in the sample. In one aspect, the composition or polynucleotide is attached to a substrate. In another aspect, the nucleic acids of the sample are amplified prior to hybridization. In yet another aspect, complex formation is compared with at least one standard and indicates the presence of a disorder.

[0013] The invention provides a purified protein or a portion thereof selected from SEQ ID NOs:49-62, which is encoded by a polynucleotide that is highly significantly co-expressed with genes known to involved in disorders associated with cardiac muscle function. The invention also provides a method for using a protein to screen a plurality of molecules to identify or to purify at least one ligand which specifically binds the protein. The molecules are selected from aptamers, DNA molecules, RNA molecules, peptide nucleic acids, peptides, mimetics, ribozymes, proteins, antibodies, agonists, antagonists, immunoglobulins, inhibitors, pharmaceutical agents or drug compounds.

[0014] The invention provides a method of using a protein to make an antibody comprising immunizing a animal with the protein under conditions to elicit an antibody response, isolating animal antibodies, attaching the protein to a substrate, contacting the substrate with isolated antibodies under conditions to allow specific binding to the protein, and dissociating the antibodies from the protein, thereby obtaining purified antibodies. The invention also provides a method for using the antibody to detect expression of a protein in a sample, the method comprising combining the antibody with a sample under conditions which allow the formation of antibody:protein complexes, and detecting complex formation, wherein complex formation indicates expression of the protein in the sample. The invention also provides a composition comprising a polynucleotide, a protein, or an antibody that specifically binds a protein and a labeling moiety or a pharmaceutical carrier.

BRIEF DESCRIPTION OF THE SEQUENCE LISTING AND TABLES

[0015] The Sequence Listing provides exemplary polynucleotide sequences, SEQ ID NOs:1-48, and polypeptide sequences, SEQ ID NOs:49-62. Each sequence is identified by a sequence identification number (SEQ ID NO) and by the Incyte clone number with which the sequence was first identified.

[0016] Table 1 presents the results of co-expression analysis. The entries in the table are the p-values which link the novel polynucleotides with known marker genes.

[0017] Table 2 shows the characterization of proteins having the amino acid sequences of SEQ ID NO:49-62.

DESCRIPTION OF THE INVENTION

[0018] It must be noted that as used herein and in the appended claims, the singular forns “a”, “an”, and “the” include the plural reference unless the context clearly dictates otherwise. Thus, for example, a reference to “a host cell” includes a plurality of such host cells, and a reference to “an antibody” is a reference to one or more antibodies and equivalents thereof known to those skilled in the art, and so forth.

[0019] Definitions

[0020] “Markers” refer to polynucleotides, proteins, and antibodies which are useful in the diagnosis, prognosis, evaluation of therapies and treatment of disorders associated with cardiac muscle function. Typically, this means that the marker gene or polynucleotide is differentially expressed in samples from subjects predisposed to, manifesting, or diagnosed with disorders associated with cardiac muscle function.

[0021] “Differential expression” refers to an increased or up-regulated or a decreased or down-regulated expression as detected by presence, absence or at least about a two-fold change in the amount of transcribed messenger RNA or protein in a sample.

[0022] “Disorders associated with cardiac muscle function” specifically include, but are not limited to, the following conditions, diseases, and disorders: atherosclerosis, arteriosclerosis, atrial fibrillation, cancer (myxoma) and complications of cancer, cardiac injury, congestive heart failure, coronary artery disease, hypertension, hypertrophic cardiomyopathy, myocardial hypertrophy, myocardial infarction, and plaque.

[0023] “Isolated or purified” refers to a polynucleotide or protein that is removed from its natural environment and that is separated from other components with which it is naturally present.

[0024] “Genes known to be highly, and differentially, expressed in cardiac muscle function” which were used in the co-expression analysis included atrial regulatory myosin, ventricular myosin alkali light chain, cardiac troponin, cardiac ventricular myosin, cardiodilatin, creatine kinase M, myoglobin, natriuretic peptide precursor, sarcomeric mitochondrial creatine kinase, telethonin, titin, and urocortin.

[0025] “Polynucleotide” refers to an isolated cDNA. It can be of genomic or synthetic origin, double-stranded or single-stranded, and combined with vitamins, minerals, carbohydrates, lipids, proteins, or other nucleic acids to perform a particular activity or form a useful composition.

[0026] “Protein” refers to a purified polypeptide whether naturally occurring or synthetic.

[0027] “Sample” is used in its broadest sense. A sample containing nucleic acids can comprise a bodily fluid; an extract from a cell; a chromosome, organelle, or membrane isolated from a cell; genomic DNA, RNA, or cDNA in solution or bound to a substrate; a cell; a tissue; a tissue print; and the like.

[0028] “Substrate” refers to any rigid or semi-rigid support to which polynucleotides or proteins are bound and includes membranes, filters, chips, slides, wafers, fibers, magnetic or nonmagnetic beads, gels, capillaries or other tubing, plates, polymers, and microparticles with a variety of surface forms including wells, trenches, pins, channels and pores.

[0029] A “transcript image” is a profile of gene transcription activity in a particular tissue at a particular time.

[0030] A “variant” refers to a polynucleotide or protein whose sequence diverges from about 5% to about 30% from the nucleic acid or amino acid sequences of the Sequence Listing.

[0031] The Invention

[0032] The present invention employed “guilt by association (GBA)”, a method for using marker genes known to be associated with cardiac muscle function to identify surrogate markers, polynucleotides that are similarly associated or co-expressed in the same tissues, pathways or disorders (Walker and Volkmuth (1999) Prediction of gene function by genome-scale expression analysis: prostate-associated genes. Genome Res 9:1198-1203, incorporated herein by reference). The genes known to be associated with cardiac muscle function are atrial regulatory myosin, ventricular myosin alkali light chain, cardiac troponin, cardiac ventricular myosin, cardiodilatin, creatine kinase M, myoglobin, natriuretic peptide precursor, sarcomeric mitochondrial creatine kinase, telethonin, titin, and urocortin. In particular, the method identifies cDNAs cloned from mRNA transcripts which were active in tissues removed from subjects with cardiac disorders including, but not limited to, atherosclerosis, arteriosclerosis, atrial fibrillation, cancer (myxoma) and complications of cancer, cardiac injury, congestive heart failure, coronary artery disease, hypertension, hypertrophic cardiomyopathy, myocardial hypertrophy, myocardial infarction, and plaque. The polynucleotides, their encoded proteins and antibodies which specifically bind to the encoded proteins are useful in the diagnosis, prognosis, evaluation of therapies, and treatment of disorders associated with cardiac muscle function. U.S. Ser. No. 09/299,708 is incorporated in its entirety by reference herein.

[0033] Guilt by association provides for the identification of polynucleotides that are expressed in a plurality of libraries. The polynucleotides represent genes of unknown function which are co-expressed in a specific pathway, disease process, subcellular compartment, cell type, tissue, or species. The expression patterns of the genes known to be highly and differentially expressed during cardiac muscle function; atrial regulatory myosin, ventricular myosin alkali light chain, cardiac troponin, cardiac ventricular myosin, cardiodilatin, creatine kinase M, myoglobin, natriuretic peptide precursor, sarcomeric mitochondrial creatine kinase, telethonin, titin, and urocortin; are compared with those of polynucleotides with unknown function to determine whether a specified co-expression probability threshold is met. Through this comparison, a subset of the polynucleotides having a high co-expression probability with the known marker genes can be identified.

[0034] The polynucleotides originate from human cDNA libraries. These polynucleotides can also be selected from a variety of sequence types including, but not limited to, expressed sequence tags (ESTs), assembled polynucleotides, full length coding regions, and 3′ untranslated regions. To be considered in GBA or co-expression analysis, the polynucleotides had to have been expressed in at least five cDNA libraries. In this application, GBA was applied to a total of 45,233 assembled polynucleotide bins that met the criteria of having been expressed in at least five libraries.

[0035] The cDNA libraries used in the co-expression analysis were obtained from adrenal gland, biliary tract, bladder, blood cells, blood vessels, bone marrow, brain, bronchus, cartilage, chromaffin system, colon, connective tissue, cultured cells, embryonic stem cells, endocrine glands, epithelium, esophagus, fetus, ganglia, heart, hypothalamus, hemic/immune system, intestine, islets of Langerhans, kidney, larynx, liver, lung, lymph, muscles, neurons, ovary, pancreas, penis, phagocytes, pituitary, placenta, pleura, prostate, salivary glands, seminal vesicles, skeleton, spleen, stomach, testis, thymus, tongue, ureter, uterus, and the like. The number of cDNA libraries analyzed can range from as few as three to greater than 10,000 and preferably, the number of the cDNA libraries is greater than 500.

[0036] In a preferred embodiment, the polynucleotides are assembled from related sequences, such as sequence fragments derived from a single transcript. Assembly of the polynucleotide can be performed using sequences of various types including, but not limited to, ESTs, extension of the EST, shotgun sequences from a cloned insert, or full length cDNAs. In a most preferred embodiment, the polynucleotides are derived from human sequences that have been assembled using the algorithm disclosed in U.S. Ser. No. 9,276,534, filed Mar. 25, 1999, and used in U.S. Ser. No. 09/226,994, filed Jan. 7, 1999, both incorporated herein by reference.

[0037] Experimentally, differential expression of the polynucleotides can be evaluated by methods including, but not limited to, differential display by spatial immobilization or by gel electrophoresis, genome mismatch scanning, representational difference analysis, and transcript imaging. For example, the results of transcript imaging for SEQ ID NOs:29 and 44 are shown in Example IX. Differential expression of SEQ ID NO:29 is highly specifically correlated with hypertension, and SEQ ID NO:44, with myocardial infarction. The transcript image provided direct confirmation of the strength of co-expression analysis--the use of known genes to identify unknown polynucleotides and their encoded proteins which are highly significantly associated with disorders associated with cardiac muscle function. Additionally, differential expression can be assessed by microarray technology. These methods can be used alone or in combination.

[0038] Genes known to be highly expressed in disorders associated with cardiac muscle function can be selected based on research in which the genes are found to be key elements of biochemical or signaling pathways or on the known use of the genes as diagnostic or prognostic markers or therapeutic targets for such disorders. Preferably, the known genes are atrial regulatory myosin, ventricular myosin alkali light chain, cardiac troponin, cardiac ventricular myosin, cardiodilatin, creatine kinase M, myoglobin, natriuretic peptide precursor, sarcomeric mitochondrial creatine kinase, telethonin, titin, and urocortin.

[0039] The procedure for identifying novel polynucleotides that exhibit a statistically significant co-expression pattern with known genes is as follows. First, the presence or absence of a polynucleotide in a cDNA library is defined: a polynucleotide is present in a cDNA library when at least one cDNA fragment corresponding to the polynucleotide is detected in a cDNA from that library, and a polynucleotide is absent from a library when no corresponding cDNA fragment is detected.

[0040] Second, the significance of co-expression is evaluated using a probability method to measure a due-to-chance probability of the co-expression. The probability method can be the Fisher exact test, the chi-squared test, or the kappa test. These tests and examples of their applications are well known in the art and can be found in standard statistics texts (Agresti (1990) Categorical Data Analysis, John Wiley & Sons, New York N.Y.; Rice (1988) Mathematical Statistics and Data Analysis, Duxbury Press, Pacific Grove Calif.). A Bonferroni correction (Rice, supra, p. 384) can also be applied in combination with one of the probability methods for correcting statistical results of one polynucleotide versus multiple other polynucleotides. In a preferred embodiment, the due-to-chance probability is measured by a Fisher exact test, and the threshold of the due-to-chance probability is set preferably to less than 0.001, more preferably to less than 0.00001.

[0041] For example, to determine whether two genes, A and B, have similar co-expression patterns, occurrence data vectors can be generated as illustrated in the table below. The presence of a gene occurring at least once in a library is indicated by a one, and its absence from the library, by a zero. Library 1 Library 2 Library 3 . . . Library N Gene A 1 1 0 . . . 0 Gene B 1 0 1 . . . 0

[0042] For a given pair of genes, the occurrence data in the table above can be summarized in a 2×2 contingency table. The second table (below) presents co-occurrence data for gene A and gene B in a total of 30 libraries. Both gene A and gene B occur 10 times in the libraries. Gene A Present Gene A Absent Total Gene B Present 8 2 10 Gene B Absent 2 18 20 Total 10 20 30

[0043] The second table summarizes and presents: 1) the number of times gene A and B are both present in a library; 2) the number of times gene A and B are both absent in a library; 3) the number of times gene A is present, and gene B is absent; and 4) the number of times gene B is present, and gene A is absent. The upper left entry is the number of times the two genes co-occur in a library, and the middle right entry is the number of times neither gene occurs in a library. The off diagonal entries are the number of times one gene occurs, and the other does not. Both A and B are present eight times and absent 18 times. Gene A is present, and gene B is absent, two times; and gene B is present, and gene A is absent, two times. The probability (“p-value”) that the above association occurs due to chance as calculated using a Fisher exact test is 0.0003.

[0044] This method of estimating the probability for co-expression makes several assumptions. The method assumes that the libraries are independent and are identically sampled. However, in practical situations, the selected cDNA libraries are not entirely independent, because more than one library can be obtained from a single subject or tissue. Nor are they entirely identically sampled, because different numbers of cDNAs can have been sequenced from each library. The number of cDNAs sequenced typically ranges from 5,000 to 10,000 cDNAs per library. After the Fisher exact co-expression probability is calculated for each polynucleotide versus all other assembled polynucleotides that occur, a Bonferroni correction for multiple statistical tests is applied.

[0045] Using the method of the present invention, we have identified polynucleotides, SEQ ID NOs:1-48 and their encoded proteins, SEQ ID NOs:49-62, that exhibit highly significant co-expression probability with known marker genes for disorders associated with cardiac muscle function. The results presented in Example VI show the direct associations among the novel polynucleotides and the known marker genes for disorders associated with cardiac muscle function. Therefore, by these associations, the novel polynucleotides are useful as surrogate markers for the co-expressed known markers in diagnosis, prognosis, evaluation of therapies and treatment of disorders associated with cardiac muscle function. Further, the proteins or peptides expressed from the novel polynucleotides are either potential therapeutics or targets for the identification and/or development of therapeutics.

[0046] In one embodiment, the present invention encompasses a composition comprising a plurality of polynucleotides having the nucleic acid sequences of SEQ ID NOs:1-48 or the complements thereof. These 48 polynucleotides are shown by the method to have significant co-expression with known markers for disorders associated with cardiac muscle function. The invention also provides a polynucleotide, its complement, a probe comprising the polynucleotide or the complement thereof selected from SEQ ID NOs:1-48.

[0047] The polynucleotide can be used to search against the GenBank primate (pri), rodent (rod), mammalian (mam), vertebrate (vrtp), and eukaryote (eukp) databases; the encoded protein, against GenPept, SwissProt, BLOCKS (Bairoch et al. (1997) Nucleic Acids Res 25:217-221), PFAM, and other databases that contain previously identified and annotated protein sequences, motifs, and gene functions. Methods that search for primary sequence patterns with secondary structure gap penalties (Smith et al. (1992) Protein Engineering 5:35-51) as well as algorithms such as Basic Local Alignment Search Tool (BLAST; Altschul (1993) J Mol Evol 36:290-300; Altschul et al. (1990) J Mol Biol 215:403410), BLOCKS (Henikoff and Henikoff (1991) Nucleic Acids Res 19:6565-6572), Hidden Markov Models (HMM; Eddy (1996) Cur Opin Str Biol 6:361-365; Sonnhammer et al. (1997) Proteins 28:405-420), and the like, can be used to manipulate and analyze nucleotide and amino acid sequences. These databases, algorithms and other methods are well known in the art and are described in Ausubel et al. (1997; Short Protocols in Molecular Biology, John Wiley & Sons, New York N.Y., unit 7.7) and in Meyers (1995; Molecular Biology and Biotechnology, Wiley VCH, New York N.Y., p 856-853).

[0048] Also encompassed by the invention are polynucleotides that are capable of hybridizing to SEQ ID NOs:1-48 and the complements thereof under highly stringent conditions. Stringency can be defined by salt concentration, temperature, and other chemicals and conditions well known in the art. Conditions can be selected, for example, by varying the concentrations of salt in the prehybridization, hybridization, and wash solutions or by varying the hybridization and wash temperatures. With some substrates, the temperature can be decreased by adding a solvent such as formamide to the prehybridization and hybridization solutions.

[0049] Hybridization can be performed at low stringency, with buffers such as 5×SSC (saline sodium citrate) with 1% sodium dodecyl sulfate (SDS) at 60 C., which permits complex formation between two nucleic acid sequences that contain some mismatches. Subsequent washes are performed at higher stringency with buffers such as 0.2×SSC with 0.1% SDS at either 45 C. (medium stringency) or 68 C. (high stringency), to maintain hybridization of only those complexes that contain completely complementary sequences. Background signals can be reduced by the use of detergents such as SDS, sarcosyl, or TRITON X-100 (Sigma-Aldrich, St. Louis Mo.), and/or a blocking agent, such as salmon sperm DNA. Hybridization methods are described in detail in Ausubel (supra, units2.8-2.11, 3.18-3.19 and 4-6-4.9) and Sambrook et al. (1989; Molecular Cloning A Laboratory Manual, Cold Spring Harbor Press, Plainview N.Y.).

[0050] A polynucleotide can be extended utilizing primers and employing various PCR-based methods known in the art to detect upstream sequences such as promoters and other regulatory elements. (See, e.g., Dieffenbach and Dveksler (1995) PCR Primer, a Laboratory Manual, Cold Spring Harbor Press, Plainview N.Y.) Commercially available kits such as XL-PCR (Applied Biosystems (ABI), Foster City Calif.), cDNA libraries (Life Technologies, Rockville Md.) or genomic libraries (Clontech, Palo Alto Calif.) and nested primers can be used to extend the sequence. For all PCR-based methods, primers can be designed using commercially available software (e.g., LASERGENE software, DNASTAR, Madison Wis. or another program), to be about 15 to 30 nucleotides in length, to have a GC content of about 50%, and to form a hybridization complex at temperatures of about 68C. to 72C.

[0051] In another aspect of the invention, the polynucleotide can be cloned into a recombinant vector that directs the expression of the protein, or structural or functional portions thereof, in host cells. Due to the inherent degeneracy of the genetic code, other DNA sequences which encode functionally equivalent amino acid sequence can be produced and used to express the protein encoded by the polynucleotide. The nucleotide sequences of the present invention can be engineered using methods generally known in the art in order to alter the nucleotide sequences for a variety of purposes including, but not limited to, modification of the cloning, processing, and/or expression of the gene product. DNA shuffling by random fragmentation, as described in U.S. Pat. No. 5,830,721, and PCR reassembly of gene fragments and synthetic oligonucleotides can be used to engineer the nucleotide sequences. For example, oligonucleotide-mediated site-directed mutagenesis can be used to introduce mutations that create new restriction sites, alter glycosylation patterns, change codon preference, produce splice variants, and so forth.

[0052] In order to express a biologically active protein, the polynucleotide or derivatives thereof, can be inserted into an expression vector with elements for transcriptional and translational control of the inserted coding sequence in a particular host. These elements include regulatory sequences, such as enhancers, constitutive and inducible promoters, and 5′ and 3′ untranslated regions. Methods which are well known to those skilled in the art can be used to construct such expression vectors. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination (Ausubel, supra, unit 16).

[0053] A variety of expression vector/host cell systems can be utilized to express the polynucleotide. These include, but are not limited to, microorganisms such as bacteria transformed with recombinant bacteriophage, plasmid, or cosmid expression vectors; yeast transformed with yeast expression vectors; insect cell systems infected with baculovirus vectors; plant cell systems transformed with viral or bacterial expression vectors; or animal cell systems. For long term production of recombinant proteins in mammalian systems, stable expression in cell lines is preferred. For example, the polynucleotide can be transformed into cell lines using expression vectors which can contain viral origins of replication and/or endogenous expression elements and a selectable or visible marker gene on the same or on a separate vector. The invention is not to be limited by the vector or host cell employed.

[0054] In general, host cells that contain the polynucleotide and that express the protein can be identified by a variety of procedures known to those of skill in the art. These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridizations, PCR amplification, and protein bioassay or immunoassay techniques which include membrane, solution, or chip-based technologies for the detection and/or quantification of nucleic acid or amino acid sequences. Immunological methods for detecting and measuring the expression of the protein using either specific polyclonal or monoclonal antibodies are known in the art. Examples of such techniques include enzyme-linked immunosorbent assays (ELISAs), radioimmunoassays (RIAs), and fluorescence activated cell sorting (FACS).

[0055] Host cells transformed with the polynucleotide can be cultured under conditions for the expression and recovery of the protein from cell culture. The protein produced by a transgenic cell can be secreted or retained intracellularly depending on the sequence and/or the vector used. As will be understood by those of skill in the art, expression vectors containing the polynucleotide can be designed to contain signal sequences which direct secretion of the protein through a prokaryotic cell wall or eukaryotic cell membrane.

[0056] In addition, a host cell strain can be chosen for its ability to modulate expression of the inserted sequences or to process the expressed protein in the desired fashion. Such modifications of the protein include, but are not limited to, acetylation, carboxylation, glycosylation, phosphorylation, lipidation, and acylation. Post-translational processing which cleaves a “prepro” form of the protein can also be used to specify protein targeting, folding, and/or activity. Different host cells which have specific cellular machinery and characteristic mechanisms for post-translational activities (e.g., CHO, HeLa, MDCK, HEK293, and WI38) are available from the ATCC (Manassas Va.) and can be chosen to ensure the correct modification and processing of the expressed protein.

[0057] In another embodiment of the invention, natural, modified, or recombinant polynucleotides are ligated to a heterologous sequence resulting in translation of a fusion protein containing heterologous protein moieties in any of the aforementioned host systems. Such heterologous protein moieties facilitate purification of fusion proteins using commercially available affinity matrices. Such moieties include, but are not limited to, glutathione S-transferase, maltose binding protein, thioredoxin, calmodulin binding peptide, 6-His, FLAG, c-myc, hemaglutinin, and monoclonal antibody epitopes.

[0058] In another embodiment, the polynucleotides, wholly or in part, are synthesized using chemical or enzymatic methods well known in the art (Caruthers et al. (1980) Nucl Acids Symp Ser (7) 215-233; Ausubel, supra, units 10.4 and 10.16). Peptide synthesis can be performed using various solid-phase techniques (Roberge et al. (1995) Science 269:202-204), and machines such as the ABI 431A peptide synthesizer (ABI) can be used to automate synthesis. If desired, the amino acid sequence can be altered during synthesis to produce a more stable variant for therapeutic use.

[0059] Screening, Diagnostics and Therapeutics

[0060] The polynucleotides can be used as surrogate markers in diagnosis, prognosis, evaluation of therapies and treatment of disorders associated with cardiac muscle function including, but not limited to, atherosclerosis, arteriosclerosis, atrial fibrillation, cancer (myxoma) and complications of cancer, cardiac injury, congestive heart failure, coronary artery disease, hypertension, hypertrophic cardiomyopathy, myocardial hypertrophy, myocardial infarction, and plaque.

[0061] The polynucleotide can be used to screen a plurality or library of molecules and compounds for specific binding affinity. The assay can be used to screen DNA molecules, RNA molecules, peptide nucleic acids, peptides, mimetics, ribozymes, or proteins including transcription factors, enhancers, repressors, and the like which regulate the activity of the polynucleotide in the biological system. The assay involves providing a plurality of molecules and compounds, combining a polynucleotide or a composition of the invention with the plurality of molecules and compounds under conditions to allow specific binding, and detecting specific binding to identify at least one molecule or compound which specifically binds at least one polynucleotides of the invention.

[0062] Similarly the proteins, or portions thereof, can be used to screen a plurality or library of molecules or compounds in any of a variety of screening assays to identify a ligand. The protein employed in such screening can be free in solution, affixed to an abiotic substrate or expressed on the external, or a particular internal surface, of a bacterial, or other, cell. Specific binding between the protein and the ligand can be measured. The assay can be used to screen aptamers, DNA molecules, RNA molecules, peptide nucleic acids, peptides, mimetics, ribozymes, proteins, antibodies, agonists, antagonists, immunoglobulins, inhibitors, pharmaceutical agents or drug compounds and the like, which specifically bind the protein. One method for high throughput screening using very small assay volumes and very small amounts of test compound is described in Burbaum et al. U.S. Pat. No. 5,876,946, incorporated herein by reference, which screens large numbers of molecules for enzyme inhibition or receptor binding.

[0063] In one preferred embodiment, the polynucleotides are used for diagnostic purposes to determine the differential expression of a gene in a sample. The polynucleotide consists of complementary RNA and DNA molecules, branched nucleic acids, and/or PNAs. In one alternative, the polynucleotides are used to detect and quantify gene expression in biopsied samples in which differential expression of the polynucleotide indicates the presence of a disorder. In another alternative, the polynucleotide can be used to detect genetic polymorphisms associated with a disease or disorder. In a preferred embodiment, these polymorphisms are detected in an mRNA transcribed from an endogenous gene.

[0064] In another preferred embodiment, the polynucleotide is used as a probe. Specificity of the probe is determined by whether it is made from a unique region, a regulatory region, or from a region encoding a conserved motif. Both probe specificity and the stringency of the diagnostic hybridization or amplification will determine whether the probe identifies only naturally occurring, exactly complementary sequences, allelic variants, or related sequences. Probes designed to detect related sequences should preferably have at least 50% sequence identity to at least a fragment of a polynucleotide of the invention.

[0065] Methods for producing hybridization probes include the cloning of nucleic acid sequences into vectors for the production of RNA probes. Such vectors are known in the art, are commercially available, and can be used to synthesize RNA probes in vitro by adding RNA polymerases and labeled nucleotides. Probes can incorporate nucleotides labeled by a variety of reporter groups including, but not limited to, radionuclides such as ³²P or ³⁵S, enzymatic labels such as alkaline phosphatase coupled to the probe via avidin/biotin coupling systems, fluorescent labels such as Cy3 and Cy5, and the like. The labeled polynucleotides can be used in Southern or northern analysis, dot blot, or other membrane-based technologies, on chips or other substrates, and in PCR technologies. Hybridization probes are also useful in mapping the naturally occurring genonic sequence. Fluorescent in situ hybridization (FISH) can be correlated with other physical chromosome mapping techniques and genetic map data as described in Heinz-ULrich et al. (In: Meyers, supra, pp. 965-968). In many cases, genomic context helps identify genes that encode a particular protein family. (See, e.g., Kirschning et al. (1997) Genomics 46:416-25.)

[0066] The polynucleotide can be labeled using standard methods and added to a sample from a subject under conditions for the formation and detection of hybridization complexes. After incubation the sample is washed, and the signal associated with complex formation is quantitated and compared with at least one standard value. Standard values are derived from any control sample, typically one that is free of the suspect disorder and from one that represents a single, specific and preferably, staged disorder. If the amount of signal in the subject sample is distinguishable from the standards, then differential expression in the subject sample indicates the presence of the disorder. Qualitative and quantitative methods for comparing complex formation in subject samples with previously established standards are well known in the art.

[0067] Such assays can also be used to evaluate the efficacy of a particular therapeutic treatment regimen in animal studies, in clinical trials, or to monitor the treatment of an individual subject. Once the presence of the disorder has been established and a treatment protocol is initiated, hybridization, amplification, or antibody assays can be repeated on a regular basis to determine when gene or protein expression in the patient begins to approximate that which is observed in a healthy subject. The results obtained from successive assays can be used to show the efficacy of treatment over a period ranging from several hours, e.g. in the case of toxic shock, to many years, e.g. in the case of osteoarthritis.

[0068] The polynucleotides can be used on a substrate such as a microarray to monitor gene expression, to identify splice variants, mutations, and polymorphisms. Information derived from analyses of expression patterns can be used to determine gene function, to understand the genetic basis of a disease, to diagnose a disorder, and to develop and monitor the activities of therapeutic agents used to treat a disorder. Microarrays can also be used to detect genetic diversity, single nucleotide polymorphisms, which may characterize a particular population, at the genomic level.

[0069] In another embodiment, antibodies or Fabs comprising an antigen binding site that specifically binds the protein can be used for the diagnosis of diseases characterized by the differential expression of the protein. A variety of protocols for measuring protein expression, including ELISAs, RIAs, FACS and antibody arrays, are well known in the art and provide a basis for diagnosing differential or abnormal levels of expression. Standard values for protein expression parallel those reviewed above for nucleotide expression. The amount of complex formation can be quantitated by various methods, preferably by photometric means. Quantities of the protein expressed in subject samples are compared with standard values. Deviation between standard and subject values establishes the parameters for diagnosing or monitoring a particular disorder. Alternatively, one can use competitive drug screening assays in which neutralizing antibodies capable of binding specifically with the protein compete with a test compound. Antibodies can be used to detect the presence of any peptide which shares one or more epitopes or antigenic determinants with the protein. In one aspect, the antibodies of the present invention can be used for treatment of a disorder, delivery of therapeutics, or monitoring therapy during treatment.

[0070] In another aspect, the polynucleotide, or its complement, can be used therapeutically for the purpose of expressing mRNA and protein, or conversely to block transcription or translation of the mRNA. Expression vectors can be constructed using elements from retroviruses, adenoviruses, herpes or vaccinia viruses, or bacterial plasmids, and the like. These vectors can be used for delivery of nucleotide sequences to a particular target cell population, tissue, or organ. Methods well known to those skilled in the art can be used to construct vectors to express the polynucleotides or their complements. (See, e.g., Maulik et al. (1997) Molecular Biotechnology, Therapeutic Applications and Strategies, Wiley-Liss, New York N.Y.)

[0071] Alternatively, the polynucleotide or its complement, can be used for somatic cell or stem cell gene therapy. Vectors can be introduced in vivo, in vitro, and ex vivo. For ex vivo therapy, vectors are introduced into stem cells taken from the subject, and the resulting transgenic cells are clonally propagated for autologous transplant back into that same subject. Delivery of the polynucleotide by transfection, liposome injections, or polycationic amino polymers can be achieved using methods which are well known in the art. (See, e.g., Goldman et al. (1997) Nature Biotechnology 15:462-466.) Additionally, endogenous gene expression can be inactivated using homologous recombination methods which insert an inactive gene sequence into the coding region or other targeted region of the genome. (See, e.g. Thomas et al. (1987) Cell 51: 503-512.)

[0072] Vectors containing the polynucleotide can be transformed into a cell or tissue to express a missing protein or to replace a nonfunctional protein. Similarly a vector constructed to express the complement of the polynucleotide can be transformed into a cell to down-regulate protein expression. Complementary or antisense sequences can consist of an oligonucleotide derived from the transcription initiation site; nucleotides between about positions −10 and +10 from the ATG are preferred. Similarly, inhibition can be achieved using triple helix base-pairing methodology. Triple helix pairing is useful because it causes inhibition of the ability of the double helix to open sufficiently for the binding of polymerases, transcription factors, or regulatory molecules. Recent therapeutic advances using triplex DNA have been described in the literature. (See, e.g., Gee et al. In: Huber and Carr (1994) Molecular and Immunologic Approaches, Futura Publishing, Mt. Kisco N.Y., pp. 163-177.)

[0073] Ribozymes, enzymatic RNA molecules, can also be used to catalyze the cleavage of mRNA and decrease the levels of particular mRNAs, such as those comprising the polynucleotides of the invention. (See, e.g., Rossi (1994) Current Biology 4: 469-471.) Ribozymes can cleave MRNA at specific cleavage sites. Alternatively, ribozymes can cleave mRNAs at locations dictated by flanking regions that form complementary base pairs with the target mRNA. The construction and production of ribozymes is well known in the art and is described in Meyers (supra).

[0074] RNA molecules can be modified to increase intracellular stability and half-life. Possible modifications include, but are not limited to, the addition of flanking sequences at the 5′ and/or 3′ ends of the molecule, or the use of phosphorothioate or 2′ O-methyl rather than phosphodiester linkages within the backbone of the molecule. Alternatively, nontraditional bases such as inosine, queosine, and wybutosine, as well as acetyl-, methyl-, thio-, and similarly modified forms of adenine, cytidine, guanine, thymine, and uridine which are not as easily recognized by endogenous endonucleases, can be included.

[0075] Further, an antagonist, or an antibody that binds specifically to the protein can be administered to a subject to treat a disorders associated with cardiac muscle function. The antagonist, antibody, or fragment can be used directly to inhibit the activity of the protein or indirectly to deliver a therapeutic agent to cells or tissues which express the protein. The therapeutic agent can be a cytotoxic agent selected from a group including, but not limited to, abrin, ricin, doxorubicin, daunorubicin, taxol, ethidium bromide, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicine, dihydroxy anthracin dione, actinomycin D, diphteria toxin, Pseudomonas exotoxin A and 40, radioisotopes, and glucocorticoid.

[0076] Antibodies to the protein can be generated using methods that are well known in the art. One method involves immunizing a animal with the protein selected from SEQ ID NOs:49-62 under conditions to elicit an antibody response; isolating animal antibodies; attaching the protein to a substrate; contacting the substrate with isolated antibodies under conditions to allow specific binding to the protein; and dissociating the antibodies from the protein, thereby obtaining purified antibodies. Such antibodies can include, but are not limited to, polyclonal, monoclonal, chimeric, and single chain antibodies, Fab fragments, and fragments produced by a Fab expression library. Neutralizing antibodies, such as those which inhibit dimer formation, are especially preferred for therapeutic use. Monoclonal antibodies to the protein can be prepared using any technique which provides for the production of antibody molecules by continuous cell lines in culture. These include, but are not limited to, the hybridoma, the human B-cell hybridoma, and the EBV-hybridoma techniques. In addition, techniques developed for the production of chimeric antibodies can be used. (See, e.g., Pound (1998) Immunochemical Protocols, Methods Mol Biol Vol. 80.) Alternatively, techniques described for the production of single chain antibodies can be employed. Fabs which contain specific binding sites for the protein can also be generated. Various immunoassays can be used to identify antibodies having the desired specificity. Numerous protocols for competitive binding or immunoradiometric assays using either polyclonal or monoclonal antibodies with established specificities are well known in the art.

[0077] Yet further, an agonist of the protein can be administered to a subject to treat a disorder associated with decreased expression, longevity or activity of the protein.

[0078] An additional aspect of the invention relates to the administration of a pharmaceutical or sterile composition, in conjunction with a pharmaceutically acceptable carrier, for any of the therapeutic applications discussed above. Such pharmaceutical compositions can consist of the protein or antibodies, mimetics, agonists, antagonists, or inhibitors of the protein. The compositions can be administered alone or in combination with at least one other agent, such as a stabilizing compound, which can be administered in any sterile, biocompatible pharmaceutical carrier including, but not limited to, saline, buffered saline, dextrose, and water. The compositions can be administered to a subject alone or in combination with other agents, drugs, or hormones.

[0079] The pharmaceutical compositions utilized in this invention can be administered by any number of routes including, but not limited to, oral, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, transdernal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual, or rectal means.

[0080] In addition to the active ingredients, these pharmaceutical compositions can contain pharmaceutically-acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically. Further details on techniques for formulation and administration can be found in the latest edition of Remington's Pharmaceutical Sciences (Mack Publishing, Easton Pa.).

[0081] For any compound, the therapeutically effective dose can be estimated initially either in cell culture assays or in animal models such as mice, rats, rabbits, dogs, or pigs. An animal model can also be used to determine the concentration range and route of administration. Such information can then be used to determine useful doses and routes for administration in humans.

[0082] A therapeutically effective dose refers to that amount of active ingredient which ameliorates the symptoms or condition. Therapeutic efficacy and toxicity can be determined by standard pharmaceutical procedures in cell cultures or with experimental animals, such as by calculating and contrasting the ED₅₀ (the dose therapeutically effective in 50% of the population) and LD₅₀ (the dose lethal to 50% of the population) statistics. Any of the therapeutic compositions described above can be applied to any subject in need of such therapy, including, but not limited to, mammals such as dogs, cats, cows, horses, rabbits, monkeys, and most preferably, humans.

[0083] Stem Cells and Their Use SEQ ID NOs:1-48 can be useful in the differentiation of stem cells. Eukaryotic stem cells are able to differentiate into the multiple cell types of various tissues and organs and to play roles in embryogenesis and adult tissue regeneration (Gearhart (1998) Science 282:1061-1062; Watt and Hogan (2000) Science 287:1427-1430). Depending on their source and developmental stage, stem cells can be totipotent with the potential to create every cell type in an organism and to generate a new organism, pluripotent with the potential to give rise to most cell types and tissues, but not a whole organism; or multipotent cells with the potential to differentiate into a limited number of cell types. Stem cells can be transfected with polynucleotides which can be transiently expressed or can be integrated within the cell as transgenes.

[0084] Embryonic stem (ES) cell lines are derived from the inner cell masses of human blastocysts and are pluripotent (Thomson et al. (1998) Science 282:1145-1147). They have normal karyotypes and express high levels of telomerase which prevent senescence and allow the cells to replicate indefinitely. ES cells produce derivatives that give rise to embryonic epidermal, mesodermal and endodermal cells. Embryonic germ (EG) cell lines, which are produced from primordial germ cells isolated from gonadal ridges and mesenteries, also show stem cell behavior (Shamblott et al. (1998) Proc Natl Acad Sci 95:13726-13731). EG cells have normal karyotypes and appear to be pluripotent.

[0085] Organ-specific adult stem cells differentiate into the cell types of the tissues from which they were isolated. They maintain their original tissues by replacing cells destroyed from disease or injury. Adult stem cells are multipotent and under proper stimulation can be used to generate cell types of various other tissues (Vogel (2000) Science 287:1418-1419). Hematopoietic stem cells from bone marrow provide not only blood and immune cells, but can also be induced to transdifferentiate to form brain, liver, heart, skeletal muscle and smooth muscle cells. Similarly mesenchymal stem cells can be used to produce bone marrow, cartilage, muscle cells, and some neuron-like cells, and stem cells from muscle have the ability to differentiate into muscle and blood cells (Jackson et al. (1999) Proc Natl Acad Sci 96:14482-14486). Neural stem cells, which produce neurons and glia, can also be induced to differentiate into heart, muscle, liver, intestine, and blood cells (Kuhn and Svendsen (1999) BioEssays 21:625-630); Clarke et al. (2000) Science 288:1660-1663; Gage (2000) Science 287:1433-1438; and Galli et al. (2000) Nature Neurosci 3:986-991).

[0086] Neural stem cells can be used to treat neurological disorders such as Alzheimer's disease, Parkinson's disease, and multiple sclerosis and to repair tissue damaged by strokes and spinal cord injuries. Hematopoietic stem cells can be used to restore immune function in immunodeficient patients or to treat autoimmune disorders by replacing autoreactive immune cells with normal cells to treat diseases such as multiple sclerosis, scleroderma, rheumatoid arthritis, and systemic lupus erythematosus. Mesenchymal stem cells can be used to repair tendons or to regenerate cartilage to treat arthritis. Liver stem cells can be used to repair liver damage. Pancreatic stem cells can be used to replace islet cells to treat diabetes. Muscle stem cells can be used to regenerate muscle to treat muscular dystrophies (Fontes and Thomson (1999) BMJ 319:1-3; Weissman (2000) Science 287:1442-1446 Marshall (2000) Science 287:1419-1421; and Marmont (2000) Ann Rev Med 51:115-134).

EXAMPLES

[0087] It is to be understood that this invention is not limited to the particular devices, machines, materials and methods described. Although particular embodiments are described, equivalent embodiments can be used to practice the invention. The described embodiments are provided to illustrate the invention and are not intended to limit the scope of the invention which is limited only by the appended claims.

[0088] cDNA Library Construction

[0089] The cDNA library, LATRNOT01, was selected as an example to demonstrate library construction. The LATRNOT01 cDNA library was constructed from left atrial tissue obtained from a 51 -year-old Caucasian female who died of cerebral hemorrhage.

[0090] The frozen tissue was homogenized using a pestle and mortar and lysed using a POLYTRON homogenizer (Brinkmann Instruments, Westbury N.Y.) in guanidinium isothiocyanate solution. The lysate was centrifuged over a 5.7 M CsCl cushion using an SW28 swinging bucket rotor in an L8-70M ultracentrifuge (Beckman Coulter, Fullerton Calif.) for 18 hours at 25,000 rpm and ambient temperature. The RNA was extracted twice with phenol, pH 8.0, precipitated using 0.3 M sodium acetate and 2.5 volumes of ethanol, resuspended in RNAse-free water, and treated with DNAse at 37C. The mRNA was isolated using the OLIGOTEX kit (Qiagen, Chatsworth Calif.) and used to construct the cDNA library.

[0091] The mRNA was handled according to the recommended protocols in the SUPERSCRIPT plasmid system (Life Technologies, Gaithersburg Md.). cDNAs were fractionated on a SEPHAROSE CL4B column (Amersham Pharmacia Biotech (APB), Piscataway N.J.), and those cDNAs exceeding 400 bp were ligated into the XhoI and EcoRI sites of the λ UNIZAP vector (Stratagene, La Jolla Calif.). The vector which contained the PBLUESCRIPT phagemid was subsequently transformed into XL1-BLUEMRF host cells (Stratagene). The phagemid forms of individual cDNA clones were obtained by the in vivo excision process, in which the host bacterial strain was co-infected with both the λ library phage and an f1 helper phage. Enzymes derived from both the library-containing and helper phage nicked the λ DNA, initiated new DNA synthesis from defined sequences on the λ target DNA, and created a smaller, single stranded circular phagemid DNA molecule that included all DNA sequences of the PBLUESCRIPT phagemid and the cDNA insert. The phagemid DNA was secreted from the cells, purified, and used to re-infect fresh host cells, where the double stranded phagemid DNA was produced.

[0092] II Isolation and Sequencing of cDNA Clones

[0093] Plasmid DNA was released from the bacterial cells and purified using the REAL PREP 96 plasmid kit (Qiagen). This kit enabled the simultaneous purification of 96 samples in a 96-well block using multi-channel reagent dispensers. The recommended protocol was employed except for the following changes: 1) the bacteria were cultured in 1 ml of sterile TERRIFIC BROTH (BD Biosciences, San Jose Calif.) with carbenicillin at 25 mg/L and glycerol at 0.4%; 2) after inoculation, the cells were culture for 19 hours and then lysed in 0.3 ml of lysis buffer; and 3) the plasmid DNA pellet was precipitated in isopropanol and then resuspended in 0.1 ml of distilled water. After the last step in the protocol, samples were transferred to a 96-well block for storage at 4 C.

[0094] The cDNAs were prepared using a MICROLAB 2200 system (Hamilton, Reno Nev.) in combination with DNA ENGINE thermal cyclers (MJ Research, Watertown Mass.). The cDNAs were sequenced by the method of Sanger and Coulson (1975; J Mol Biol 94:441-448) using ABI PRISM 373, 377 or 3700 DNA sequencing systems (ABI). Most of the cDNAs were sequenced using standard ABI protocols and kits at solution volumes of 0.25x-1.0x. In the alternative, some of the cDNAs were sequenced using solutions and dyes from APB.

[0095] III Selection, Assembly, and Characterization of Sequences

[0096] The polynucleotides used for co-expression analysis were assembled from EST sequences, 5′ and 3′ long read sequences, and full length coding sequences. The assembly process is described as follows. EST sequence chromatograms were processed and verified. Quality scores were obtained using PHRED (Ewing et al. (1998) Genome Res 8:175-185; Ewing and Green (1998) Genome Res 8:186-194), and edited sequences were loaded into a relational database management system (RDBMS). The sequences were clustered using BLAST with a product score of 50. All clusters of two or more sequences created a bin which represents one transcribed gene.

[0097] Assembly of the component sequences within each bin was performed using a modification of Phrap, a publicly available program for assembling DNA fragments (Green, P. University of Washington, Seattle Wash.). Bins that showed 82% identity from a local pair-wise alignment between any of the consensus sequences were merged.

[0098] Bins were annotated by screening the consensus sequence in each bin against public databases, such as GBpri and GenPept from NCBI. The annotation process involved a FASTn screen against the GBpri database in GenBank. Those hits with a percent identity of greater than or equal to 75% and an alignment length of greater than or equal to 100 base pairs were recorded as homolog hits. The residual unannotated sequences were screened by FASTx against GenPept. Those hits with an E value of less than or equal to 10⁻⁸ were recorded as homolog hits.

[0099] Sequences were then reclustered using BLASTn and Cross-Match, a program for rapid amino acid and nucleic acid sequence comparison and database search (Green, supra), sequentially. Any BLAST alignment between a sequence and a consensus sequence with a score greater than 150 was realigned using cross-match. The sequence was added to the bin whose consensus sequence gave the highest Smith-Waterman score (Smith et al. (1992) Protein Engineering 5:35-51) amongst local alignments with at least 82% identity. Non-matching sequences were moved into new bins, and assembly processes were repeated.

[0100] IV Homology Searching of Polynucleotides and Their Encoded Proteins

[0101] The polynucleotides of the Sequence Listing or their encoded proteins were used to query databases such as GenBank, SwissProt, BLOCKS, and the like. These databases that contain previously identified and annotated sequences or domains were searched using BLAST or BLAST 2 (Altschul et al. supra; Altschul, supra) to produce alignments and to determine which sequences were exact matches or homologs. The alignments were to sequences of prokaryotic (bacterial) or eukaryotic (animal, fungal, or plant) origin. Alternatively, algorithms such as the one described in Smith and Smith (1992, Protein Engineering 5:35-51) could have been used to deal with primary sequence patterns and secondary structure gap penalties. All of the sequences disclosed in this application have lengths of at least 49 nucleotides, and no more than 12% uncalled bases (where N is recorded rather than A, C, G, or T).

[0102] As detailed in Karlin and Altschul (1993; Proc Natl Acad Sci 90:5873-5877), BLAST matches between a query sequence and a database sequence were evaluated statistically and only reported when they satisfied the threshold of 10⁻²⁵ for nucleotides and 10⁻¹⁴ for peptides. Homology was also evaluated by product score calculated as follows: the % nucleotide or amino acid identity [between the query and reference sequences] in BLAST is multiplied by the % maximum possible BLAST score [based on the lengths of query and reference sequences] and then divided by 100. In comparison with hybridization procedures used in the laboratory, the electronic stringency for an exact match was set at 70, and the conservative lower limit for an exact match was set at approximately 40 (with 1-2% error due to uncalled bases).

[0103] The BLAST software suite, freely available sequence comparison algorithms (NCBI, Bethesda Md.; http://www.ncbi.nlm.nih.gov/gorf/12.html), includes various sequence analysis programs including “blastn” that is used to align nucleic acid molecules and BLAST 2 that is used for direct pairwise comparison of either nucleic or amino acid molecules. BLAST programs are commonly used with gap and other parameters set to default settings, e.g.: Matrix: BLOSUM62; Reward for match: 1; Penalty for mismatch: -2; Open Gap: 5 and Extension Gap: 2 penalties; Gap x drop-off: 50; Expect: 10; Word Size: 11; and Filter: on. Identity or similarity is measured over the entire length of a sequence or some smaller portion thereof. Brenner et al. (1998; Proc Natl Acad Sci 95:6073-6078, incorporated herein by reference) analyzed the BLAST for its ability to identify structural homologs by sequence identity and found 30% identity is a reliable threshold for sequence alignments of at least 150 residues and 40%, for alignments of at least 70 residues.

[0104] The polynucleotides of this application were compared with assembled consensus sequences or templates found in the LIFESEQ GOLD database. Component sequences from cDNA, extension, full length, and shotgun sequencing projects were subjected to PHRED analysis and assigned a quality score. All sequences with an acceptable quality score were subjected to various pre-processing and editing pathways to remove low quality 3′ ends, vector and linker sequences, polyA tails, Alu repeats, mitochondrial and ribosomal sequences, and bacterial contamination sequences. Edited sequences had to be at least 50 bp in length, and low-information sequences and repetitive elements such as dinucleotide repeats, Alu repeats, and the like, were replaced by “Ns” or masked.

[0105] Edited sequences were subjected to assembly procedures in which the sequences were assigned to polynucleotide bins. Each sequence could only belong to one bin, and sequences in each bin were assembled to produce a template. Newly sequenced components were added to existing bins using BLAST and CROSSMATCH. To be added to a bin, the component sequences had to have a BLAST quality score greater than or equal to 150 and an alignment of at least 82% local identity. The sequences in each bin were assembled using PHRAP. Bins with several overlapping component sequences were assembled using DEEP PHRAP. The orientation of each template was determined based on the number and orientation of its component sequences.

[0106] Bins were compared to one another and those having local similarity of at least 82% were combined and reassembled. Bins having templates with less than 95% local identity were split. Templates were subjected to analysis by STITCHER/EXON MAPPER algorithms that analyze the probabilities of the presence of splice variants, alternatively spliced exons, splice junctions, differential expression of alternative spliced genes across tissue types or disease states, and the like. Assembly procedures were repeated periodically, and templates were annotated using BLAST against GenBank databases such as GBpri. An exact match was defined as having from 95% local identity over 200 base pairs through 100% local identity over 100 base pairs and a homolog match as having an E-value (or probability score) of <1×10⁻⁸. The templates were also subjected to frameshift FASTx against GENPEPT, and homolog match was defined as having an E-value of <1×10⁻⁸. Template analysis and assembly was described in U.S. Ser. No. 09/276,534, filed Mar. 25, 1999.

[0107] Following assembly, templates were subjected to BLAST, motif, and other functional analyses and categorized in protein hierarchies using methods described in U.S. Ser. Nos. 08/812,290 and 08/811,758, both filed Mar. 6, 1997; in U.S. Ser. No. 08/947,845, filed Oct. 9, 1997; and in U.S. Ser. No. 09/034,807, filed Mar. 4, 1998. Then templates were analyzed by translating each template in all three forward reading frames and searching each translation against the PFAM database of hidden Markov model-based protein families and domains using the HMMER software package (Washington University School of Medicine, St. Louis Mo.; http://pfam.wustl.edu/).

[0108] The polynucleotide was further analyzed using MACDNASIS PRO software (Hitachi Software Engineering), and LASERGENE software (DNASTAR) and queried against public databases such as the GenBank rodent, mammalian, vertebrate, prokaryote, and eukaryote databases, SwissProt, BLOCKS, PRINTS, PFAM, and Prosite.

[0109] V Description of Known Cardiac Muscle-Associated Genes

[0110] Twelve known cardiac muscle-associated genes were selected to identify novel polynucleotides that are closely associated with cardiac muscle function. These known genes were atrial regulatory myosin, ventricular myosin alkali light chain, cardiac troponin, cardiac ventricular myosin, cardiodilatin, creatine kinase M, myoglobin, natriuretic peptide precursor, sarcomeric mitochondrial creatine kinase, telethonin, titin, and urocortin.

[0111] Brief descriptions of the known cardiac muscle-associated genes and their expression in cardiac disorders are presented below. GENE DESCRIPTION AND REFERENCES atrial regulatory Predominant regulatory myosin light chain myosin isoform in adult atrial muscle. Differentially expressed in cardiovascular development and disease. Fewell et al. (1998) J Clin Invest 101:2630-2639; Hailstones et al. (1992) J. Biol. Chem. 267:23295-23300. ventricular myosin Muscle fiber protein. Differentially expressed in alkali light chain altered cardiovascular function and in myocardial hypertrophy. Morano et al. (1997) J Mol Cell Cardiol 29:1177-1187. troponin Marker of cardiac injury. Feng et al. (1998) Am J Clin Pathol 110:70-77; Luscher et al. (1998) Cardiology 89:222-228; and Kost et al. (1998) Arch Pathol Lab Med 122:245-251. cardiac ventricular Muscle fiber protein. Expressed in cardiac myosin remodeling after myocardial infarction. Differentially expressed in altered cardiovascular function. Trahair et al. (1993) J Mol Cell Cardiol 25:577-585. cardiodilatin Differentially expressed following myocardial infarction. Induces vasorelaxation. Gidh-Jain et al. (1998) J Mol Cell Cardiol 30:627-637; Magga et al. (1998) Ann Med 30(S1):39-45. creatine kinase M Marker of cardiac injury. Feng, supra; Luscher, supra; and Kost, supra. myoglobin Marker of cardiac injury. Feng, supra; Luscher, supra; and Kost, supra. natriuretic peptide See cardiodilatin. precursor sarcomeric Essential enzyme in energy metabolism, mitochondrial creatine particularly in tissue with high energy kinase requirements. Klein et al. (1991) J Biol Chem 266:18058-18065; Qin et al. (1997) J Biol Chem 272:25210-25216. telethonin Sarcomeric protein of heart and skeletal muscle. Valle et al. (1997) FEBS Lett. 415:163-168; Mayans et al. (1998) Nature 395:863-869. titin Muscle fiber protein. Temporal and spatial control of sarcomere assembly. Differentially expressed after atrial fibrillation. Ausma et al. (1997) Am J Pathol 151:985-997; Mayans, supra. urocortin Stimulates atrial natriuretic peptide secretion. Expression increased following cardiac injury. Protects cardiac myocytes from hypoxic death. Ikeda et al. (1998) Biochem. Biophys Res Commun 250:298-304; Asaba et al. (1998) Brain Res 806:95-103; and Okosi et al. (1998) Neuropeptides 32:167-171.

[0112] VI Co-Expression Among Known Marker Genes and Novel Polynucleotides

[0113] GBA identified 48 novel polynucleotides from a total of 45,233 assembled sequences that showed strong expression and association with the known cardiac muscle-associated genes. The process was reiterated until the number of polynucleotides was reduced to the final 48 polynucleotides shown below. Each of the 48 polynucleotides is co-expressed with at least one of the twelve known genes with a p-value of less than 10⁻⁰⁵.

[0114] The co-expression of the novel polynucleotides and the known genes are shown in Table 1-1, 1-2, and 1-3. The novel polynucleotides are listed along the top of the table by their SEQ ID NO, and the known genes, by their names in the rows down the side of the table. The entries in the table are the negative log of the p-value (−log p) for the co-expression of two sequences. For each polynucleotide, the p-value is the probability that the observed co-expression is due to chance, using the Fisher Exact Test.

[0115] The highest co-expression value is obtained when the highest p-value found in a vertical column below the SEQ ID NO (clone number) is correlated with the name of a known marker gene listed for that row. For example, SEQ ID NO:4, has a p-value of 19 as it co-expresses with cardiac ventricular myosin. This highly significant p-value substantiates that SEQ ID NO:4, SEQ ID NO:49, and an antibody which specifically binds SEQ ID NO:49 can be used as surrogate markers for cardiac ventricular myosin in a diagnostic assay for myocardial infarction.

[0116] The data above can be summarized by reducing it to a single highest co-expression (−log p) value for each intersecting known gene and unknown polynucleotide and naming at least one disorder associated with expression of the known gene. A summary table is shown below: SEQ ID p- NO value Gene Disorder 1 7 atrial regulatory myosin cardiac injury 2 6 natriuretic peptide precursor myocardial infarction 3 7 telethonin atrial fibrillation 4 19 cardiac ventricular myosin myocardial infarction 5 9 creatine kinase M cardiac injury 6 11 titin atrial fibrillation 7 10 troponin cardiac injury 8 6 natriuretic peptide precursor myocardial infarction 9 6 urocortin myocardial infarction 10 12 telethonin atrial fibrillation 11 8 creatine kinase M cardiac injury 12 9 atrial regulatory myosin cardiac injury 13 22 titin atrial fibrillation 14 8 ventricular myosin alkali light myocardial hypertrophy chain 15 10 titin atrial fibrillation 16 7 titin atrial fibrillation 17 8 telethonin atrial fibrillation 18 6 urocortin myocardial infarction 19 11 creatine kinase M cardiac injury 20 13 myoglobin cardiac injury 21 10 ventricular myosin alkali light myocardial hypertrophy chain 22 10 troponin cardiac injury 23 11 titin atrial fibrillation 24 7 ventricular myosin alkali light myocardial hypertrophy chain 25 9 ventricular myosin alkali light myocardial hypertrophy chain 26 18 creatine kinase M cardiac injury 27 19 ventricular myosin alkali light myocardial hypertrophy chain 28 21 creatine kinase M cardiac injury 29 5 sarcomeric mitoch. creatine hypertension kinase 30 15 myoglobin cardiac injury 31 7 telethonin atrial fibrillation 32 8 creatine kinase M cardiac injury 33 11 titin atrial fibrillation 34 9 atrial regulatory myosin cardiac injury 35 8 creatine kinase M cardiac injury 36 7 cardiac ventricular myosin myocardial infarction 37 16 myoglobin cardiac injury 38 11 myoglobin cardiac injury 39 21 creatine kinase M cardiac injury 40 11 creatine kinase M cardiac injury 41 20 creatine kinase M cardiac injury 42 8 titin atrial fibrillation 43 6 cardiac ventricular myosin myocardial infarction 44 7 cardiodilantin myocardial infarction 45 10 telethonin atrial fibrillation 46 11 creatine kinase M cardiac injury 47 9 atrial regulatory myosin cardiac injury 48 9 telethonin atrial fibrillation

[0117] VII Description of the Polynucleotides Identified Using GBA

[0118] Using the method of Walker (supra), 48 polynucleotides that exhibit strong association, or co-expression, with cardiac muscle-associated genes have been identified.

[0119] Polynucleotides comprising the nucleic acid sequences of SEQ ID NOs:1-48 of the present invention fied as Incyte Clones 2045674, 188552, 465676, 3601719, 305781, 971441, 3445829, 189299, 2396760, 919893, 2837330, 1737459, 058201, 767447, 5449893, 2951269, 282977, 3178454, 3563859, 985730, 3684987, 986166, 1887508, 1006416, 975169, 4152861, 986464, 118472, 1314633, 1997439, 2638878, 3795510, 1413537, 1623157, 3009303, 3434460, 5022769, 944140, 3445829, 3016490, 4151935, 3719652, 3046106, 3012947, 466761, 1644171, 3009806, and 5578191, respectively; and assembled according to Example III. As described in Example IV, BLAST and other motif searches were performed for each sequence. SEQ ID NOs:1-48 were translated, and identity with known sequences was sought. Proteins comprising SEQ ID NOs:49-62 were also analyzed using BLAST and other motif search tools as disclosed in Example VI. The details of the various analyses are described in Table 2.

[0120] VIII Hybridization Technologies and Analyses

[0121] Immobilization of Polynucleotides on a Substrate

[0122] The polynucleotides are applied to a substrate by one of the following methods. A mixture of polynucleotides is fractionated by gel electrophoresis and transferred to a nylon membrane by capillary transfer. Alternatively, the polynucleotides are individually ligated to a vector and inserted into bacterial host cells to form a library. The polynucleotides are then arranged on a substrate by one of the following methods. In the first method, bacterial cells containing individual clones are robotically picked and arranged on a nylon membrane. The membrane is placed on LB agar containing selective agent (carbenicillin, kanamycin, ampicillin, or chloramphenicol depending on the vector used) and incubated at 37 C. for 16 hr. The membrane is removed from the agar and consecutively placed colony side up in 10% SDS, denaturing solution (1.5 M NaCl, 0.5 M NaOH), neutralizing solution (1.5 M NaCl, 1 M Tris-HCl, pH 8.0), and twice in 2×SSC for 10 min each. The membrane is then UV irradiated in a STRATALINKER UV-crosslinker (Stratagene).

[0123] In the second method, polynucleotides are amplified from bacterial vectors by thirty cycles of PCR using primers complementary to vector sequences flanking the insert. PCR amplification increases a starting concentration of 1-2 ng nucleic acid to a final quantity greater than 5 μg. Amplified nucleic acids from about 400 bp to about 5000 bp in length are purified using SEPHACRYL-400 beads (APB). Purified nucleic acids are arranged on a nylon membrane manually or using a dot/slot blotting manifold and suction device and are immobilized by denaturation, neutralization, and UV irradiation as described above. Purified nucleic acids are robotically arranged and immobilized on polymer-coated glass slides using the procedure described in U.S. Pat. No. 5,807,522. Polymer-coated slides are prepared by cleaning glass microscope slides (Corning, Acton Mass.) by ultrasound in 0.1% SDS and acetone, etching in 4% hydrofluoric acid (VWR Scientific Products, West Chester Pa.), coating with 0.05% aminopropyl silane (Sigma-Aldrich) in 95% ethanol, and curing in a 110 C. oven. The slides are washed extensively with distilled water between and after treatments. The nucleic acids are arranged on the slide and then immobilized by exposing the array to UV irradiation using a STRATALINKER UV-crosslinker (Stratagene). Arrays are then washed at room temperature in 0.2% SDS and rinsed three times in distilled water. Non-specific binding sites are blocked by incubation of arrays in 0.2% casein in phosphate buffered saline (PBS; Tropix, Bedford Mass.) for 30 min at 60 C.; then the arrays are washed in 0.2% SDS and rinsed in distilled water as before.

[0124] Probe Preparation for Membrane Hybridization

[0125] Hybridization probes derived from the polynucleotides of the Sequence Listing are employed for screening cDNAs, mRNAs, or genomic DNA in membrane-based hybridizations. Probes are prepared by diluting the polynucleotides to a concentration of 40-50 ng in 45 μl TE buffer, denaturing by heating to 100 C. for five min, and briefly centrifuging. The denatured polynucleotide is then added to a REDIPRIME tube (APB), gently mixed until blue color is evenly distributed, and briefly centrifuged. Five μl of [³²P]dCTP is added to the tube, and the contents are incubated at 37 C. for 10 min. The labeling reaction is stopped by adding 5 μl of 0.2M EDTA, and probe is purified from unincorporated nucleotides using a PROBEQUANT G-50 microcolumn (APB). The purified probe is heated to 100 C. for five min, snap cooled for two min on ice, and used in membrane-based hybridizations as described below.

[0126] Probe Preparation for Polymer Coated Slide Hybridization

[0127] Hybridization probes derived from mRNA isolated from samples are employed for screening polynucleotides of the Sequence Listing in array-based hybridizations. Probe is prepared using the GEMbright kit (Incyte Genomics) by diluting mRNA to a concentration of 200 ng in 9 μl TE buffer and adding 5 μl 5×buffer, 1 μl 0.1 M DTT, 3 μl Cy3 or Cy5 labeling mix, 1 μl RNAse inhibitor, 1 μl reverse transcriptase, and 5 μl 1×yeast control mRNAs. Yeast control mRNAs are synthesized by in vitro transcription from noncoding yeast genomic DNA (W. Lei, unpublished). As quantitative controls, one set of control mRNAs at 0.002 ng, 0.02 ng, 0.2 ng, and 2 ng are diluted into reverse transcription reaction mixture at ratios of 1:100,000, 1:10,000, 1:1000, and 1:100 (w/w) to sample mRNA respectively. To examine mRNA differential expression patterns, a second set of control mRNAs are diluted into reverse transcription reaction mixture at ratios of 1:3, 3:1, 1:10, 10:1, 1:25, and 25:1 (w/w). The reaction mixture is mixed and incubated at 37 C. for two hr. The reaction mixture is then incubated for 20 min at 85 C., and probes are purified using two successive CHROMA SPIN+TE 30 columns (Clontech, Palo Alto Calif.). Purified probe is ethanol precipitated by diluting probe to 90 μl in DEPC-treated water, adding 2 μl 1 mg/ml glycogen, 60 μl 5 M sodium acetate, and 300 μl 100% ethanol. The probe is centrifuged for 20 min at 20,800×g, and the pellet is resuspended in 12 μl resuspension buffer, heated to 65 C. for five min, and mixed thoroughly. The probe is heated and mixed as before and then stored on ice. Probe is used in high density array-based hybridizations as described below.

[0128] Membrane-based Hybridization

[0129] Membranes are pre-hybridized in hybridization solution containing 1% Sarkosyl and 1×high phosphate buffer (0.5 M NaCl, 0.1 M Na₂HPO₄, 5 mM EDTA, pH 7) at 55 C. for two hr. The probe, diluted in 15 ml fresh hybridization solution, is then added to the membrane. The membrane is hybridized with the probe at 55 C. for 16 hr. Following hybridization, the membrane is washed for 15 min at 25 C. in 1 mM Tris (pH 8.0), 1% Sarkosyl, and four times for 15 min each at 25 C. in 1 mM Tris (pH 8.0). To detect hybridization complexes, XOMAT-AR film (Eastman Kodak, Rochester N.Y.) is exposed to the membrane overnight at −70 C., developed, and examined visually.

[0130] Polymer Coated Slide-based Hybridization

[0131] Probe is heated to 65 C. for five min, centrifuged five min at 9400 rpm in a 5415 C. microcentrifuge (Eppendorf Scientific, Westbury N.Y.), and then 18 μl are aliquoted onto the array surface and covered with a coverslip. The arrays are transferred to a waterproof chamber having a cavity just slightly larger than a microscope slide. The chamber is kept at 100% humidity internally by the addition of 140 μl of 5×SSC in a corner of the chamber. The chamber containing the arrays is incubated for about 6.5 hr at 60 C. The arrays are washed for 10 min at 45 C. in 1×SSC, 0.1% SDS, and three times for 10 min each at 45 C. in 0.1×SSC, and dried.

[0132] Hybridization reactions are performed in absolute or differential hybridization formats. In the absolute hybridization format, probe from one sample is hybridized to array elements, and signals are detected after hybridization complexes form. Signal strength correlates with probe mRNA levels in the sample. In the differential hybridization format, differential expression of a set of genes in two biological samples is analyzed. Probes from the two samples are prepared and labeled with different labeling moieties. A mixture of the two labeled probes is hybridized to the array elements, and signals are examined under conditions in which the emissions from the two different labels are individually detectable. Elements on the array that are hybridized to equal numbers of probes derived from both biological samples give a distinct combined fluorescence (Shalon WO95/35505).

[0133] Hybridization complexes are detected with a microscope equipped with an INNOVA 70 mixed gas 10 W laser (Coherent, Santa Clara Calif.) capable of generating spectral lines at 488 nm for excitation of Cy3 and at 632 nm for excitation of Cy5. The excitation laser light is focused on the array using a 20× microscope objective (Nikon, Melville N.Y.). The slide containing the array is placed on a computer-controlled X-Y stage on the microscope and raster-scanned past the objective with a resolution of 20 micrometers. In the differential hybridization format, the two fluorophores are sequentially excited by the laser. Emitted light is split, based on wavelength, into two photomultiplier tube detectors (PMT R1477, Hamamatsu Photonics Systems, Bridgewater N.J.) corresponding to the two fluorophores. Appropriate filters positioned between the array and the photomultiplier tubes are used to filter the signals. The emission maxima of the fluorophores used are 565 nm for Cy3 and 650 nm for Cy5. The sensitivity of the scans is calibrated using the signal intensity generated by the yeast control mRNAs added to the probe mix. A specific location on the array contains a complementary DNA sequence, allowing the intensity of the signal at that location to be correlated with a weight ratio of hybridizing species of 1:100,000.

[0134] The output of the photomultiplier tube is digitized using a 12-bit RTI-835H analog-to-digital (A/D) conversion board (Analog Devices, Norwood Mass.) installed in an IBM-compatible PC computer. The digitized data are displayed as an image where the signal intensity is mapped using a linear 20-color transformation to a pseudocolor scale ranging from blue (low signal) to red (high signal). The data is also analyzed quantitatively. Where two different fluorophores are excited and measured simultaneously, the data are first corrected for optical crosstalk (due to overlapping emission spectra) between the fluorophores using the emission spectrum for each fluorophore. A grid is superimposed over the fluorescence signal image such that the signal from each spot is centered in each element of the grid. The fluorescence signal within each element is then integrated to obtain a numerical value corresponding to the average intensity of the signal. The software used for signal analysis is the GEMTOOLS program (Incyte Genomics).

[0135] IX Transcript Imaging

[0136] The transcript image performed using the LIFESEQ GOLD database (Aug00rel, Incyte Genomics) allowed assessment of the relative abundance of expressed polynucleotides in one or more cDNA libraries. Criteria for transcript imaging include category, number of cDNAs per library, description of the library, and the like

[0137] All sequences and cDNA libraries in the LIFESEQ database were categorized by system, organ/tissue and cell type. The categories included cardiovascular system, connective tissue, digestive system, embryonic structures, endocrine system, exocrine glands, female and male reproductive, germ cells, hemic/immune system, liver, musculoskeletal system, nervous system, pancreas, respiratory system, sense organs, skin, stomatognathic system, unclassified/mixed, and the urinary tract. For each category, the number of libraries in which the sequence was expressed were counted and shown over the total number of libraries in that category. In some transcript images, all normalized or pooled libraries, which have high copy number sequences removed prior to processing, and all mixed or pooled tissues, which are considered non-specific in that they contain more than one tissue type or more than one subject's tissue, can be excluded from the analysis. Cell lines and/or fetal tissue data can also be disregarded unless the elucidation of inherited disorders would be furthered by their inclusion in the analysis.

[0138] For diagnostic purposes, the standards to which biopsied samples would be compared are: cytologically normal, non-diseased samples versus samples which had been diagnosed with specific cardiac disorders including, but not limited to, atherosclerosis, arteriosclerosis, atrial fibrillation, cancer (myxoma) and complications of cancer, cardiac injury, congestive heart failure, coronary artery disease, hypertension, hypertrophic cardiomyopathy, myocardial hypertrophy, myocardial infarction, and plaque.

[0139] For purposes of example, the transcript images for SEQ ID NOs:29 and 44 are shown below. The first column shows library name; the second column, the number of cDNAs sequenced in that library; the third column, the description of the library; and the fourth column, absolute abundance of the transcript in the library. SEQ ID NO:29 (Category: Cardiovascular*) Abun- % Abun- Library cDNA Description dance dance HEARNOT06 3685 heart, hypertension, 44M 2 0.0543 HEARFET05 2524 heart, fetal, M 1 0.0396 HEARFET02 6919 heart, hypoplastic 1 0.0145 left, fetal, 23wM

[0140] SEQ ID NO:44 (Category: Cardiovascular*) Abun- % Abun- Library cDNA Description dance dance HEALDIT02 4171 left ventricle, mw/ 1 0.0240 myocardial infarction, 56M HEARFET02 6919 heart, hypoplastic left, 1 0.0145 fetal, 23wM

[0141] SEQ ID NOs:29 and 44 were differentially expressed when compared by percent abundance to useful standards (i.e., the up-regulation of SEQ ID NOs:29 in heart tissue of a deceased victim who was shot to death is not a comparison that would be made in a diagnostic setting). More importantly, these sequences are not differentially expressed in any normal tissue or diagnostic of any other cardiac disorder.

[0142] The differential expression of SEQ ID NOs:29, and 44, respectively, in tissue associated with hypertension and myocardial infarction, respectively, supports the use of the sequences as a surrogate markers for sarcomeric mitochondrial creatine kinase and cardiodilantin, respectively. These transcript images verify GBA analysis (see Example VI above).

[0143] X Complementary Molecules

[0144] The complement of the novel polynucleotide, from about 5 bp (e.g., a PNA) to about 5000 bp (e.g., the complement of a cDNA insert), are used to detect or inhibit gene expression. These molecules are selected using LASERGENE software (DNASTAR). Detection is described in Example VIII. To inhibit transcription by preventing promoter binding, the complementary molecule is designed to bind to the most unique 5′ sequence and includes nucleotides of the 5′ UTR upstream of the initiation codon of the open reading frame. Complementary molecules include genomic sequences (such as enhancers or introns) and are used in “triple helix” base pairing to compromise the ability of the double helix to open sufficiently for the binding of polymerases, transcription factors, or regulatory molecules. To inhibit translation, a complementary molecule is designed to prevent ribosomal binding to the mRNA encoding the protein.

[0145] Complementary molecules are placed in expression vectors and used to transform a cell line to test efficacy; into an organ, tumor, synovial cavity, or the vascular system for transient or short term therapy; or into a stem cell, zygote, or other reproducing lineage for long term or stable gene therapy. Transient expression lasts for a month or more with a non-replicating vector and for three months or more if appropriate elements for inducing vector replication are used in the transformation/expression system.

[0146] Stable transformation of appropriate dividing cells with a vector encoding the complementary molecule produces a transgenic cell line, tissue, or organism (U.S. Pat. No. 4,736,866). Those cells that assimilate and replicate sufficient quantities of the vector to allow stable integration also produce enough complementary molecules to compromise or entirely eliminate activity of the polynucleotide encoding the protein.

[0147] XI Protein Expression

[0148] Expression and purification of the protein are achieved using either a cell expression system or an insect cell expression system. The pUB6/V5-His vector system (Invitrogen, Carlsbad Calif.) is used to express protein in CHO cells. The vector contains the selectable bsd gene, multiple cloning sites, the promoter/enhancer sequence from the human ubiquitin C gene, a C-terminal V5 epitope for antibody detection with anti-V5 antibodies, and a C-terminal polyhistidine (6×His) sequence for rapid purification on PROBOND resin (Invitrogen). Transformed cells are selected on media containing blasticidin.

[0149]Spodoptera frugiperda (Sf9) insect cells are infected with recombinant Autographica californica nuclear polyhedrosis virus (baculovirus). The polyhedrin gene is replaced with the polynucleotide by homologous recombination and the polyhedrin promoter drives transcription. The protein is synthesized as a fusion protein with 6×his which enables purification as described above. Purified protein is used in the following activity and to make antibodies.

[0150] XII Production of Antibodies

[0151] The protein is purified using polyacrylamide gel electrophoresis and used to immunize mice or rabbits. Antibodies are produced using the protocols below. Alternatively, the amino acid sequence of the expressed protein is analyzed using LASERGENE software (DNASTAR) to determine regions of high antigenicity. An antigenic epitope, usually found near the C-terminus or in a hydrophilic region is selected, synthesized, and used to raise antibodies. Typically, epitopes of about 15 residues in length are produced using an ABI 431A peptide synthesizer (ABI) using FMOC-chemistry and coupled to KLH (Sigma-Aldrich) by reaction with N-maleimidobenzoyl-N-hydroxysuccinimide ester to increase antigenicity.

[0152] Rabbits are immunized with the epitope-KLH complex in complete Freund's adjuvant. Immunizations are repeated at intervals thereafter in incomplete Freund's adjuvant. After a minimum of seven weeks for mouse or twelve weeks for rabbit, antisera are drawn and tested for antipeptide activity. Testing involves binding the peptide to plastic, blocking with 1% bovine serum albumin, reacting with rabbit antisera, washing, and reacting with radio-iodinated goat anti-rabbit IgG. Methods well known in the art are used to determine antibody titer and the amount of complex formation.

[0153] XIII Purification of Naturally Occuring Protein Using Specific Antibodies

[0154] Naturally occurring or recombinant protein is purified by immunoaffinity chromatography using antibodies which specifically bind the protein. An immunoaffinity column is constructed by covalently coupling the antibody to CNBr-activated SEPHAROSE resin (APB). Media containing the protein is passed over the immunoaffinity column, and the column is washed using high ionic strength buffers in the presence of detergent to allow preferential absorbance of the protein. After coupling, the protein is eluted from the column using a buffer of pH 2-3 or a high concentration of urea or thiocyanate ion to disrupt antibody/protein binding, and the protein is collected.

[0155] XIV Screening Molecules for Specific Binding Using Polynucleotide or Protein

[0156] The polynucleotide, or fragments thereof, or the protein, or portions thereof, are labeled with ³²P-dCTP, Cy3-dCTP, or Cy5-dCTP (APB), or with BIODIPY or FITC (Molecular Probes, Eugene Oreg.), respectively. Libraries of candidate molecules or compounds previously arranged on a substrate are incubated in the presence of composition, a labeled polynucleotide or protein. After incubation under conditions for either a nucleic acid or amino acid sequence, the substrate is washed, and any position on the substrate retaining label, which indicates specific binding or complex formation, is assayed, and the ligand is identified. Data obtained using different concentrations of the nucleic acid or protein are used to calculate affinity between the labeled nucleic acid or protein and the bound molecule.

[0157] XV Two-Hybrid Screen

[0158] A yeast two-hybrid system, MATCHMAKER LexA Two-Hybrid system (Clontech Laboratories, Palo Alto Calif.), is used to screen for peptides that bind the protein of the invention. A polynucleotide encoding the protein is inserted into the multiple cloning site of a pLexA vector, ligated, and transformed into E. coli. cDNA, prepared from mRNA, is inserted into the multiple cloning site of a pB42AD vector, ligated, and transformed into E. coli to construct a cDNA library. The pLexA plasmid and pB42AD-cDNA library constructs are isolated from E. coli and used in a 2:1 ratio to co-transform competent yeast EGY48 [p8op-lacZ] cells using a polyethylene glycol/lithium acetate protocol. Transformed yeast cells are plated on synthetic dropout (SD) media lacking histidine (-His), tryptophan (-Trp), and uracil (-Ura), and incubated at 30 C. until the colonies have grown up and are counted. The colonies are pooled in a minimal volume of 1×TE (pH 7.5), replated on SD/-His/-Leu/-Trp/-Ura media supplemented with 2% galactose (Gal), 1% raffinose (Raf), and 80 mg/ml 5-bromo-4-chloro-3-indolyl β-d-galactopyranoside (X-Gal), and subsequently examined for growth of blue colonies. Interaction between expressed protein and cDNA fusion proteins activates expression of a LEU2 reporter gene in EGY48 and produces colony growth on media lacking leucine (-Leu). Interaction also activates expression of β-galactosidase from the p8op-lacZ reporter construct that produces blue color in colonies grown on X-Gal.

[0159] Positive interactions between expressed protein and cDNA fusion proteins are verified by isolating individual positive colonies and growing them in SD/-Trp/-Ura liquid medium for 1 to 2 days at 30 C. A sample of the culture is plated on SD/-Trp/-Ura media and incubated at 30 C. until colonies appear. The sample is replica-plated on SD/-Trp/-Ura and SD/-His/-Trp/-Ura plates. Colonies that grow on SD containing histidine but not on media lacking histidine have lost the pLexA plasmid. Histidine-requiring colonies are grown on SD/Gal/Raf/X-Gall-Trp/-Ura, and white colonies are isolated and propagated. The pB42AD-cDNA plasmid, which contains a polynucleotide encoding a protein that physically interacts with the protein, is isolated from the yeast cells and characterized.

[0160] All patents and publications mentioned in the specification are incorporated by reference herein. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention that are obvious to those skilled in the field of molecular biology or related fields are intended to be within the scope of the following claims. TABLE 1-1 GENE NAME\SEQ ID NO* 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 atrial regulatory myosin 7 5 3 13 2 2 10 5 1 7 5 9 7 3 1 2 ventricular myosin alkali light chain 5 4 4 18 8 9 9 4 2 11 6 6 14 8 5 4 troponin 6 5 5 10 3 1 10 5 1 8 7 8 6 2 1 0 cardiac ventricular myosin 4 4 3 19 6 9 7 4 2 8 7 5 17 5 7 5 cardiodilatin 4 3 4 10 2 1 5 3 1 4 5 7 4 1 1 0 creatine kinase M 6 4 6 16 9 9 7 4 2 10 8 6 21 6 8 5 myoglobin 4 4 6 17 8 10 7 4 2 9 5 8 19 3 9 3 natriuretic peptide precursor 6 6 2 9 0 1 5 6 1 5 2 6 4 1 2 1 sarcomeric mitoch. creatine kinase 7 4 7 16 7 5 8 4 2 11 6 6 12 3 5 2 telethonin 4 4 7 15 6 8 8 4 2 12 6 5 18 6 7 6 titin 4 4 6 18 9 11 5 4 2 11 8 5 22 5 10 7 urocortin 2 1 1 7 2 5 3 1 6 5 2 2 5 2 6 6

[0161] TABLE 1-2 GENE NAME\SEQ ID NO* 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 atrial regulatory myosin 2 2 4 10 7 8 1 6 6 11 15 7 2 12 1 2 ventricular myosin alkali light chain 6 1 10 8 10 6 5 7 9 15 19 17 2 11 5 4 troponin 2 0 4 5 5 10 0 6 5 9 14 7 3 9 0 0 cardiac ventricular myosin 7 2 9 9 8 5 6 5 7 14 16 18 4 10 6 7 cardiodilatin 1 0 2 7 5 5 1 4 3 6 8 5 1 9 0 1 creatine kinase M 7 0 11 9 7 7 7 7 7 18 17 21 4 14 4 8 myoglobin 7 2 9 13 8 7 10 5 7 14 16 20 3 15 6 6 natriuretic peptide precursor 3 1 4 5 9 3 1 2 5 6 12 5 1 10 1 2 sarcomeric mitoch. creatine kinase 6 0 10 9 7 8 5 5 6 14 13 15 5 13 5 6 telethonin 8 1 9 9 7 8 9 3 8 14 16 19 1 14 7 7 titin 5 2 10 12 9 7 11 6 5 16 15 18 4 14 6 7 urocortin 3 6 5 4 4 3 4 1 3 6 6 3 2 8 6 4

[0162] TABLE 1-3 GENE NAME\SEQ ID NO* 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 atrial regulatory myosin 8 9 1 5 10 11 9 3 11 4 3 2 5 7 9 3 ventricular myosin alkali light chain 7 7 6 5 14 8 13 11 18 5 4 3 8 10 9 9 troponin 6 8 3 4 10 10 10 4 10 4 5 3 3 8 5 2 cardiac ventricular myosin 6 7 8 7 14 7 16 10 15 6 6 4 6 11 8 7 cardiodilatin 4 4 2 1 6 10 5 2 8 6 5 7 3 5 2 2 creatine kinase M 8 7 8 4 13 8 21 11 20 7 3 4 7 11 7 6 myoglobin 8 7 5 4 16 11 20 9 19 6 5 6 8 9 8 7 natriuretic peptide precursor 5 4 1 1 4 6 8 2 7 2 1 2 4 5 3 4 sarcomeric mitoch. creatine kinase 9 5 7 3 13 8 19 7 17 5 4 4 7 9 8 5 telethonin 10 7 6 4 9 6 20 10 19 4 4 2 10 8 7 9 titin 11 7 8 5 11 7 17 9 19 8 3 4 9 11 8 6 urocortin 2 4 3 3 9 3 7 3 7 1 1 2 4 3 7 6

[0163] TABLE 2 Potential SEQ ID Amino Acid Potential Phosphorylation glycosylation Analytical NO: Residues Sites sites Signature Sequence Identification Methods 49 70 S46 Motif 50 552 S541 S11 S15 S26 S54 S99 S108 N148 N174 K402 to T456 Tropomodulin Motif, BLAST T118 S125 S134 S168 T197 T250 N177 N223 Synapsins synapsin BLOCKS S312 S502 S520 T56 S77 T143 N325 T281 S392 S400 T409 S435 S499 S511 S533 51 260 S35 S51 T124 S171 S183 Y154 Motif 52 364 T103 T125 T247 T274 S329 S5 N4 M1 to G49 Signal Receptor Motif, SigPept S162 S242 S282 Peptide glycosyl PRINTS, BLOCKS m42 TO c64 and D76 hydrolase to C88 receptor signatures F173 to F182 Glycosyl hydrolases signature 53 527 S168 S232 S239 T314 S315 T332 Motif T344 T373 T496 T512 S524 54 82 T63 T67 N29 Motif 56 193 S4 S6 T60 S86 S148 T157 T60 N2 L86 to Y122 HET-C, Motif, BLAST T126 Phosphatase glycolipid BLOCKS_DOMO transforming 61K transfer protein PDF1 57 174 T49 S40 T72 S81 S21 S57 S141 N19 L8 to L29leucine CNN, mitosin, Motif, BLAST zipper pattern tropomyosin BLOCKS, PRINTS Y27 to E42 and E103 to L118 secretin receptor E54 to K71 and E103 to E131 tropomysin receptor Q95 to T148 tropomysin 58 230 S27 T33 S58 T75 T209 S23 Glycosyl Motif, BLOCKS Glycosaminoglycan Transferase attachement site P84 TO p95 Aminoacyl tRNA synthetase class-1 signature V119 to H129 glycosyl transferase signature 59 915 T775 T56 S58 S74 T100 S140 N426 N633 L530 to S641 and Ring finger Motif, BLAST S224 T240 S241 S291 T292 S308 P650 to S734 fn protein, PRINTS, BLOCKS, S314 T320 S353 S367 T375 S382 family, L607 to zincfinger Pfam S414 T422 S428 S455 T480 T502 Y625 and Y718 to protein RFP S503 S513 S529 T608 T674 S767 E732 fibronectin fibronectin T796 T20 T179 S329 T343 T361 V627 to G636 and T369 S406 S538 S641 T668 S740 F720 to G729 T849 S911 Y119 Y360 receptor glycoprotein signature 60 163 S125 S94 F74 to A93 smooth Smooth muscle Motif, muscle protein 22 protein, BLOCKS_DOMO G83 to S94 proteoglycan PRINTS proteoglycan C- terminal 62 329 S68 T67 T284 S318 N316 R28 “RGD” cell Cardiac ankyrin Motif, BLAST, attachment sequence repeat protein PRINTS, BLOCKS, L154 to L169, M187 Pfam to L202, L220 to F235, G249 to R258, and L253 to L268 ankyrin repeats

[0164]

1 62 1 790 DNA Homo sapiens misc_feature Incyte ID No 2045674CT1 1 ctgttgctcg agcccttagc aatatatacg taaacatatc cagcttgtct aacacatcac 60 agattattag ttaacaaggt gtagattaat gagcttatat tgtattgctg gatcttttga 120 gttaataaca atggtaactt gtccagaagg cctatcatca ttcctagtag gtgggcacag 180 agtaagagat attaagaagc ttcctgatga gtcatcatct agcgaaggcc ctgtgtaggg 240 ctttattata ggagttacat tgacttctgg ggcattcaaa ggtctcccct cttatccata 300 tctctgtcat tttgcccacc tactaggaat gatgataggc tttaataaca atggtaactt 360 gtccagaagg cctatcatca ttcctagtag gtgggcacag agtaagagat attaagaagc 420 ttcctgatga gtcatcatct agcgaaggcc ctgtgtaggg ctatgttata ggagttacat 480 tgacttctgg ggcattcaaa ggtctcccct cttatccata tctctgtcat tttgcttctc 540 cagccacgac aacacacttt cctctccaac tgctccctcc ccaccaaaaa agaagaccct 600 ctaaaaggca aaggaataaa tattcttaga agtaaagtat cttcatacat gctgcctttt 660 tcaaagaggt gttaggatat ttatcctatt tctgtatttc acagtagctt ttcaggctgt 720 cctgcttatg tataagctga tttctcgtgc cgaattcttg cctcgagggc caaattccct 780 atatgatcgt 790 2 459 DNA Homo sapiens misc_feature Incyte ID No 188552CT1 2 ggcacgagct gacatgagtc tcagtgccgg caaacacggc tggttgaacc ctgagctagc 60 ccagctgctt tgttcacctt acgtttgggg aaggctgaaa ttttattgag caccgactgt 120 attccacaca ctcttctagg tgcccgaaat atgctgttaa acaaatactc agccctcatg 180 gggctgagag tctggtgggg aagacctgtt gaaaaacaat catattaaat gaattgcatt 240 gcatgttaga agatcgtaag tactctgggg gaaaatgaga gtagaacagg ataagggggt 300 gatggaggga atgagtggtg attttaaatg tagttatcag gctgggcaca atggcttaca 360 cctgtaatcc cagcattttg gaaggccaag acgggcaggt cacttgaagt caggagtttg 420 agaccagcct ggccaacatg gtgaaaacct gtctctact 459 3 517 DNA Homo sapiens misc_feature Incyte ID No 465676CT1 3 gtggccagag ccagccagca tggccaccct caagaggcga gatgagccca cagaggcata 60 tcctgcgggg atgctgggct cccagtgtgg ttggcctgaa caaaataaag tgttgactcc 120 tgggcatctg tgccttctct atggccttgc tacctgggat tccagagagt tgatggggtg 180 cagatagggg taggactgtt agaatagaac caacccaaac tgtgtgtagt ttggggtgta 240 tacttctatt tctcttccta catgtctaca tgccatgacc ttcctcctcc tcttcacttg 300 gccagtttca gctcacttcc tccaggaagt ctttcctgat atatcaaact gaaacaaatg 360 ctcctcctcc atgctccctt aatccccatg cttgtcgatt atattccttt gccaattcat 420 ttctctatcc tgtctatgta taagtgtgta caagcattca agaaactgat gaatgatgaa 480 tgaatgaatg agccaaagaa caaataaatg agcccct 517 4 824 DNA Homo sapiens misc_feature Incyte ID No 3601719CB1 4 gtttaagttc ccctccagcc ccgagccagg agcagttctc aataccggga gaggcacaga 60 gctatttcag ccacatgaaa agcatcggaa ttgagatcgc agctcagagg acaccgggcg 120 ccccttccac cttccaagga gctttgtatt cttgcatctg gctgcctggg acttccctta 180 ggcagtaaac aaatacataa agcagggata agactgcatg aatatgtcga aacagccagt 240 ttccaatgtt agagccatcc aggcaaatat caatattcca atgggagcct ttcggccagg 300 agcaggtcaa ccccccagaa gaaaagaatg tactcctgaa gtggaggagg gtgttcctcc 360 cacctcggat gaggagaaga agccaattcc aggagcgaag aaacttccag gacctgcagt 420 caatctatcg gaaatccaga atattaaaag tgaactaaaa tatgtcccca aagctgaaca 480 gtagtaggaa gaaaaaagga ttgatgtgaa gaaataaaga ggcagaagat ggattcaata 540 gctcactaaa attttatata tttgtatgat gattgtgaac ctcctgaatg cctgagactc 600 tagcagaaat ggcctgtttg tacatttata tctcttcctt ctagttggct gtatttctta 660 ctttatcttc atttttggca cctcacagaa caaattagcc cataaattca acacctggag 720 ggtgtggttt tgaggaggga tatgatttta tggagaatga tatggcaatg tgcctaacga 780 ttttgatgaa aagtttccca agctacttcc tacagtattt tggt 824 5 969 DNA Homo sapiens misc_feature Incyte ID No 305781CT1 5 cccttttttt tttttttttt tttttttttt tttttttttt ttttttggga gtatagatta 60 tgtttatttt ctctataatt tccagggttt tccaaaattt tacaacaaac atctataatt 120 ttatgaacac tccccatctt atttttaaaa agaaaaaagt tggggggcag agaaatgccc 180 agctcagtac tgagatccat caagtgaggc cagccggtat ctgtcacacc aggcagaggc 240 cccgtgctgg aagccctgga ggttaccagc tccaagcctg gtatccaagg cctcctgggc 300 agccttagcc tcctccttcc ctttcctccc accagaccct gctcctggga tgtccttctc 360 ccattaccac cacaaaatcg gactaatttt tcagggccca acaccaattc tgctaatttt 420 tttttggctc aatcttggct catcacaacc tccgcctccc aggttcaacg gattctccca 480 cctcggcctt ctgaatagcc gggattacag gcacctgcca ccacgcctgg ctaatttttg 540 tatttttagt agagaccggg ttttgccatg ttggccacgc tggtctccaa ctcctgacct 600 caggtgatct gcccgccttg gcctcccaat ctccttccat ttattagttg gattgcttaa 660 aaaaaaaaaa gactccccga tatgggcagg agcaatgctg attttttact tacctgtctc 720 tagataatga attgattgtt agcctccaaa gatgatcaat ttgtttttgt ttttgttttt 780 gtttcagatt acggtgaact catggactta aacttcttta tgggttttga gccactgcaa 840 ttatcctcac caaatctcaa gctgtcccac ctctggcacg tggggcctct tcaagttttc 900 ctcattcata tttgtttgtc tgtttgttgt ttttgggtgg ccagcaggag agcatccaca 960 gtctgtctc 969 6 597 DNA Homo sapiens misc_feature Incyte ID No 971441CT1 6 aagaggtaag cgtggcctga cctagccacc caccaacagg aataatggct gaaaaagcgg 60 ggtctacatt ttcacacctt ctggttccta ttcttctcct gattggctgg attgtgggct 120 gcatcataat gatttatgtt gtcttctctt agaaaggcaa gaagatatca gattgacatc 180 atttagaaga attaagaaaa ctatgaacat gactgattat taaatgtctc atgttaaaca 240 atgcaatgtt tgacatcact ttacaaactt ggatcataaa ctggcacttt ggtatgcata 300 agaatttctt caggacaata agaaattatg agtgaatttc tctatattct gagtgagaaa 360 aatgtttagc tgtgatgaaa aatgcatgtc attaaaaaaa gtttgataaa tttaatcaca 420 ttacaaaaaa ttatcccccc ttccctctgg aaaaaactat agagaaagtg ggctgaggct 480 gtgcaaggtg gctcatgcct gtaatcccag cactttgtga ggatcctttg agcccagaaa 540 ttggagacct tcctaggcga cagagagaga ccccatctct acaaaaaaaa aaaaaaa 597 7 1918 DNA Homo sapiens misc_feature Incyte ID No 3445829CB1 7 cagcctgcca cttgcctccc tgcctgcttc tggctgcctt gaatgcctgg tccttcaagc 60 tccttctggg tctgacaaag cagggaccat gtctaccttt ggctaccgaa gaggactcag 120 taaatacgaa tccatcgacg aggatgaact cctcgcctcc ctgtcagccg aggagctgaa 180 ggagctagag agagagttgg aagacattga acctgaccgc aaccttcccg tggggctaag 240 gcaaaagagc ctgacagaga aaacccccac agggacattc agcagagagg cactgatggc 300 ctattgggaa aaggagtccc aaaaactctt ggagaaggag aggctggggg aatgtggaaa 360 ggttgcagaa gacaaagagg aaagtgagga agagcttatc tttactgaaa gtaacagtga 420 ggtttctgag gaagtgtata cagaggagga ggaggaggag tcccaggagg aagaggagga 480 agaagacagt gacgaagagg aaagaacaat tgaaactgca aaagggatta atggaactgt 540 aaattatgat agtgtcaatt ctgacaactc taagccaaag atatttaaaa gtcaaataga 600 gaacataaat ttgaccaatg gcagcaatgg gaggaacaca gagtccccag ctgccattca 660 cccttgtgga aatcctacag tgattgagga cgctttggac aagattaaaa gcaatgaccc 720 tgacaccaca gaagtcaatt tgaacaacat tgagaacatc acaacacaga cccttacccg 780 ctttgctgaa gccctcaagg acaacactgt ggtgaagacg ttcagtctgg ccaacacgca 840 tgccgacgac agtgcagcca tggccattgc agagatgctc aaagtcaatg agcacatcac 900 caacgtaaac gtcgagtcca acttcataac gggaaagggg atcctggcca tcatgagagc 960 tctccagcac aacacggtgc tcacggagct gcgtttccat aaccagaggc acatcatggg 1020 cagccaggtg gaaatggaga ttgtcaagct gctgaaggag aacacgacgc tgctgaggct 1080 gggataccat tttgaactcc caggaccaag aatgagcatg acgagcattt tgacaagaaa 1140 tatggataaa cagaggcaaa aacgtttgca ggagcaaaaa cagcaggagg gatacgatgg 1200 aggacccaat cttaggacca aagtctggca aagaggaaca cctagctctt caccttatgt 1260 atctcccagg cactcaccct ggtcatcccc aaaactcccc aaaaaagtcc agactgtgag 1320 gagccgtcct ctgtctcctg tggccacacc tcctcctcct ccccctcctc ctcctcctcc 1380 ccctccttct tcccaaaggc tgccaccacc tcctcctcct ccccctcctc cactcccaga 1440 gaaaaagctc attaccagaa acattgcaga agtcatcaaa caacaggaga gtgcccaacg 1500 ggcattacaa aatggacaaa aaaagaaaaa agggaaaaag gtcaagaaac agccaaacag 1560 tattctaaag gaaataaaaa attctctgag gtcagtgcaa gagaagaaaa tggaagacag 1620 ttcccgacct tctaccccac agagatcagc tcatgagaat ctcatggaag caattcgggg 1680 aagcagcata aaacagctaa agcgggtaag taaccagaga acagacatag gggcacagat 1740 aaagtaaatg agttgtcctc cattgcatgg tggtaccaaa gtcacctctc acaatactta 1800 tcaatacttt caatatttta gtatgcgaga gcaaacacac caagtttgaa acattaggag 1860 caggcacaca agtgagcaca tttctatttg agaggaacgc ctgggccgct ttcccagg 1918 8 1079 DNA Homo sapiens misc_feature Incyte ID No 189299CT1 8 gtcaagctct acctgagcga caaccacctc aatagcctgc ctccggagct ggggcagcta 60 cagaacctgc agattctggc cttggatttc aacaacttca aggctctgcc ccaggtggtg 120 tgcaccttga aacagctctg catcctctac ctgggcaaca acaaactctg cgacctcccc 180 agtgagctga gcctgctcca gaacctcagg accctgtgga tcgaggccaa ctgcctcacc 240 cagctgccgg atgtggtctg tgagctgagt ctccttaaga ctctgcatgc cggctccaac 300 gccctgcgtt tgctgccagg ccagctccgg cgcctccagg agctgaggac catctggctc 360 tcgggcaacc ggctaactga ctttcccact gtgctgcttc acatgccctt cctggaggtg 420 attgatgtgg actggaacag catccgttac ttccccagcc tggcgcacct gtcaagtctg 480 aagctggtca tctatgacca caatccttgc aggaacgcac ccaaggtggc caaaggtgtg 540 cgccgtgtgg ggagatgggc agaggagacg ccagagcccg accctagaaa agccaggcgc 600 tatgcgttgg tcagagagga aagccaggag ctacaggcac cagtccctct acttcctcct 660 accaactcct gaggagcttc agttgcaagt caatgccaag gacccaactg cagcatgttc 720 tggaagcctc tccattggag tggaaaggat ggctctgggt catttgggag tggctctgct 780 agtagagact gatggagaga gccaggtgga atgccataaa tcacactgag aaaatatttc 840 tggcaaacag ctcctctttc agaggggagt tgtgtgccca atgatggcat gacaaatcca 900 gagatcataa cttcctttgc gaagaagaac agctcgtcca cagcattgta tttttggaga 960 cacttgaaag agccaaaaga ggggcttggg aaacatcctg aaacctccct ggaagtctct 1020 caggaaattt gacttgggca ttggaggctc cattgggctc cttccaatta aggggtgtt 1079 9 1028 DNA Homo sapiens misc_feature Incyte ID No 2396760CT1 9 gtactgactc actataggga atttgcgcct cgaggcaaga attcggcacg aggggctgtt 60 accaggacaa ccggagcgat tgaccgttat ctgcggtttg gagccgttag cgggagaggc 120 agagatattc agaggtcttt taggatgtgc taaagggtcg tgagggctct cttaaaattt 180 tcttcacaag cggttatcca gtcgtgcccc gcggccctgc tgctggcccc ggggatctga 240 gtcgtaccct cttgtttttc tctgagtcag tcttaaggtg aaatgaagtg tggcccagtg 300 gctcctcact gtcgcttctc tagttttctg cctcctttta gaaaattgaa ttgaaaagac 360 aggatgaagt ggacacagca tgtgaagaca attctttcaa gaagtttggc tgtcaaggaa 420 aacagagaat gtgctaaaga acatacagac acagagcaga caggccacct ttgcaaccac 480 atggaggttt gtctgatatt gaagctaaag aagctaagct ggaagacaga gagaccaagt 540 cctgatgaca ttgtttgaac ccagagatcc agacatgcct gaaaactagt tttaccactg 600 gacttatccg ttgaatgagc caataaactc tcttttatac ttaaccttgg gttttacctg 660 gatttttgtc attgacagct caaaatattc taatatagaa gtatacatca ttaaatcaac 720 atttcttttt ttctctgtct tattttaaat gtaactctat aaggtactct aaaagtattc 780 tacagtctca ctaagttaat ctgcaaattt ggtaaaattc caatattaat cccaaaagta 840 ttttaagagc ttgtttttgt tgtttgcttg tttgggacta aacagaatta ctccaaaatt 900 cattgagaga aaaaaaaaac atgaaaaaaa aaacaagaaa atagaattca taaaaggaaa 960 ttgtattata taacaaagca taaaacaaga ataataaaca tagagtggta atggaataaa 1020 tagaacac 1028 10 1149 DNA Homo sapiens misc_feature Incyte ID No 919893CT1 10 tcgttctcac tgagcacgat attaggctct ctcccaactc actctattct gtcctcactc 60 ctgttttgat ttttctcttg ccatgtttga aatgttttat gggaatgtat tagaactctt 120 ttcttctaag gactgagact tccaggggat tgccatctta cctgtctctt ctccatgagg 180 gagaaggaag cagctagcta tgtccctagc tgcaggaagc ccctattttt tccaagcacg 240 aagccaccag tctcccccag ggagcatcag gaagggacat ggatgtgctc ctgccacagg 300 gcccttccta cctttggatc tgtgagaagg tgaatacaaa gcagcaggca gagtaaaatc 360 tgctgggact gcctggagat ttgtcaggag ctgcagacaa gtaccttgga gcattctgtt 420 atttttggaa agttcaaata tgcagggaca aggaggttgc tgactgtact gacaggctct 480 aagtcatttt ctccaaaaac tatctattca attatcaggg gctggtcttg aggaaggaaa 540 aaaaaaaaaa acgttcccag aattcagttt ccaaaatctc tttttaaagg gtttacacac 600 acacacacac acacacacac acacacacac acacacacac gatcattaaa aagtgtatgc 660 tctttaagaa gaaaagtaaa atatctcaaa ggacggtttc accaccgtcc tttattgaat 720 caatttttct acatttcaga gcaagtgtag attctgaggg actcctattt gccaaaaaga 780 caaaactagc aaaaaaaaaa acaaaaaaac aaaaaaaaaa ccacttaaaa ggtagcagga 840 aaagaaggta gttttgagtg tggttcactc agtgtctgtg agtctggtgt agtgtcagga 900 gtaaggccgt gtctagctca agtttacatt tggatgtcct acaacactaa acaaaatttt 960 tcataatcca tggtggggag cacactttgg agctacattt cttgtctcct cattgttgac 1020 attaattaaa catttatagg ccaggcacag tggctcacgc ctgttatccc agcactttgg 1080 gaggccgagg caggtgaatc acctgaggtc aggagtttga aaccagcctg gccaatatgg 1140 tgaaaccca 1149 11 1467 DNA Homo sapiens misc_feature Incyte ID No 2837330CB1 11 ctaaggctta tagattgcca gcctgctcag cgtctctaac ccttttcagg tctctgctgg 60 tggttctgaa gccaaacctc tgatcttcac atttgtcccc actgtcagaa gactaccaac 120 ccatactcag ttggctgaca cctctaaatt ccttgttaaa attccagaag aatcaagtga 180 taagagtcca gaaactgtaa ataggtctaa atccaatgac tacttgacct tgaatgctgg 240 gagccaacaa gagagagacc aagcgaaatt gacttgtcct tcagaggtca gtggaacgat 300 tttacaagaa agggaattcg aagcaaacaa acttcaaggg atgcagcaaa gtgacctctt 360 caaagctgaa tatgtcctta ttgtggactc cgaaggggaa gatgaggctg caagcagaaa 420 agttgaacaa ggccccccag gggggaattg gcaccgcagc tgtccggccc aagtctctag 480 ctatctcgtc cagtctggtc tctgatgtag tgcgtcccaa aacacagggg actgatctca 540 agacctcatc acatcctgaa atgcttcatg ggatggcccc tcagcaaaag catgggcagc 600 aatacaagac caagtcaagc tacaaggctt ttgcagcatt ccctacaaac acattgcttt 660 tggaacagaa gactcctaca actcttccaa gagcagctgg tcgagaaacc aaatatgcaa 720 atctctcctc accaacttct acagtatctg agagtcagct gactaagcct ggagtaattc 780 gcccagtacc tgtaaaatcc agaatattac tgaaaaaaga ggaggaagtc tatgaaccca 840 accctttcag taaatacttg gaagataaca gcgacctctt ttctgaacag gatgtaacag 900 tccctcccaa gcctgtctcg ctccatcctt tatatcagac taaactctat cctcctgcta 960 agtcactgct gcatccacag accctctcac atgctgactg tcttgcccca ggacccttca 1020 gtcatctgtc cttctccttg agtgatgaac aggagaattc tcacaccctc ctcagtcaca 1080 acgcatgcaa caagctgagt catccaatgg tggctattcc tgaacatgaa gctcttgatt 1140 ccaaagagca atgaagttgg agcagaggct gaaaacacag gctgctgaag ttttttggaa 1200 tgctggtgct aaccacttgc tagatttaac tttttttttt ttttccagaa tgagtgctcc 1260 ctttatgagt gcagtgcagc agaaccaaaa aaaaagtttg ctgcaattat atagcatcac 1320 agtgctctgc taacagccag catagaagag atttacctac agctttttgc accactgttc 1380 tagcctttaa tgccttctac ttaatattaa gctgaccgca atactaacgt gcccctatat 1440 ttggcagcca aataaagaag aatcgtg 1467 12 1691 DNA Homo sapiens misc_feature Incyte ID No 1737459CB1 12 cggctcgagg agaaagaggt ttttaaattc tccatgaagt gtactatgtt ccatcattcc 60 ttcccaaagc caccggaagc attccttcta ggaaaggtgg agtcggtagt gagaagccgg 120 aggtgagaag acccctgagc ggatggattc attcattttc tgaatttcct atgtgaggac 180 agtattagag cccagtgagg ctttgagagg ccccaaagat gagcgccaac agtagcagag 240 tgggccagct tctcttgcag ggttcagcgt gcattaggtg gaagcaggat gtggaagggg 300 ctatctacca cctagccaac tgcctcttac tcctgggctt catggggggc agtggggtgt 360 atggatgctt ctatcttttt ggcttcctga gtgcaggtta cctgtgctgc gtgctgtggg 420 gctggttcag tgcctgtggc ctggacattg ttctttggag cttcctgctg gctgtggtct 480 gcctgctcca gctggcacac ctggtatacc gtctgcgtga ggacaccctc cctgaggagt 540 ttgacctcct ctacaagacg ctgtgcctgc ccttgcaggt gcccctacag acatacaagg 600 agattgttca ctgctgtgag gagcaggtct taactctggc cactgaacag acctatgctg 660 tggagggtga gacacccatc aaccgcctgt ccctgctgct ctctggccgg gttcgtgtga 720 gccaggatgg gcagtttctg cactacatct ttccatacca gttcatggac tctcctgagt 780 gggaatcact acagccttct gaggaggggg tgttccaggt cactctgact gctgagacct 840 catgtagcta catttcctgg ccccggaaaa gtctccatct tcttctgacc aaagagcgat 900 acatctcctg cctcttctcg gctctgctgg gatatgacat ctcggagaag ctctacactc 960 tcaatgacaa gctctttgct aagtttgggc tgcgctttga catccgcctt cccagcctct 1020 accatgtcct gggtcccact gctgcagatg ctggaccaga gtccgagaag ggtgatgagg 1080 aagtctgtga gccagctgtg tcccctcctc aggccacacc cacctctctc cagcaaacac 1140 ccccttgttc tacccctcca gctaccacca actttcctgc acctcctacc cgggccaggt 1200 tgtccaggcc agacagtggc atactggctt ctagaattcc tctccagagc tactctcaag 1260 ttatatccag gggacaggcc cctttggctc caacccacac gcctgaactt taaggatcat 1320 tggactatct tctctgtggc cagcgcagct ctcttctgtg ttcacagaat ggccactgat 1380 aggcacgcct cttttcccac ccactggaag gctcacaggc aaggtgagag aggacacaga 1440 aggtgccaac actgtcgcta cagtaaggac ctgaagtgac tttgagaaat tcaccctcac 1500 aaaccttcct tcaggagcag gcattggtag tgcagaggca cagattccgt cctttaccag 1560 ctgcagaatc ttgggcaagt tacatagcct ctgtgagcct catcggtaaa cagtgggggt 1620 tatgaaaccc acctcacagg gttgttgtga ggatccaatg agttgattta ggtaagcacc 1680 tagcacatgc c 1691 13 2379 DNA Homo sapiens misc_feature Incyte ID No 058201CB1 13 cccaggatct gctctgaaac caggtctcta agtgaacatt tctcaggcat ggatgcattt 60 gagagtcaaa ttgttgagtc gaagatgaaa acctcttcat cacatagctc agaagctggc 120 aaatctggct gtgacttcaa gcatgcccca ccaacctatg aggatgtcat tgctggacat 180 attttagata tctctgattc acctaaagaa gtaagaaaaa attttcaaaa gacgtggcaa 240 gagagtggaa gagtttttaa aggcctggga tatgcaaccg cagatgcttc tgcaacatga 300 gatgagaacc accttccaag aggaatctgc atttataagt gaagctgctg ctccaagaca 360 aggaaatatg tatactttgt caaaagacag tttatccaat ggagtgccta gtggcagaca 420 agcagaattt tcataagtcc tgcttccgat gccaccattg caacagtaaa ctaagtttgg 480 gaaattatgc atcacttcat ggacaaatat actgtaaacc tcactttaaa caacttttca 540 aatccaaagg aaattatgat gaaggttttg gacataagca gcataaagat agatggaact 600 gcaaaaacca aagcagatca gtggacttta ttcctaatga agaaccaaat atgtgtaaaa 660 atattgcaga aaacaccctt gtacctggag atcgtaatga acatttagat gctggtaaca 720 gtgaagggca aaggaatgat ttgagaaaat taggggaaag gggaaaatta aaagtcattt 780 ggcctccttc caaggagatc cctaagaaaa ccttaccctt tgaggaagag ctcaaaatga 840 gtaaacctaa gtggccacct gaaatgacaa ccctgctatc ccctgaattt aaaagtgaat 900 ctctgctaga agatgttaga actccagaaa ataaaggaca aagacaagat cactttccat 960 ttttgcagcc ttatctacag tccacccatg tttgtcagaa agaggatgtt ataggaatca 1020 aagaaatgaa aatgcctgaa ggaagaaaag atgaaaagaa ggaaggaagg aagaatgtgc 1080 aagataggcc gagtgaagct gaagacacaa agagtaacag gaaaagtgct atggatctta 1140 atgacaacaa taatgtgatt gtgcagagtg ctgaaaagga gaaaaatgaa aaaactaacc 1200 aaactaatgg tgcagaagtt ttacaggtta ctaacactga tgatgagatg atgccagaaa 1260 atcataaaga aaatttgaat aagaataata ataacaatta tgtagcagtc tcatatctga 1320 ataattgcag gcagaagaca tctattttag aatttcttga tctattaccc ttgtcgagtg 1380 aagcaaatga cactgcaaat gaatatgaaa ttgagaagtt agaaaataca tctagaatct 1440 cagagttact tggtatattt gaatctgaaa agacttattc gaggaatgta ctagcaatgg 1500 ctctgaagaa acagactgac agagcagctg ctggcagtcc tgtgcagcct gctccaaaac 1560 caagcctcag cagaggcctt atggtaaagg ggggaagttc aatcatctct cctgatacaa 1620 atctcttaaa cattaaagga agccattcaa agagcaaaaa tttacacttt ttcttttcta 1680 acaccgtgaa aatcactgca ttttccaaga aaaatgagaa cattttcaat tgtgatttaa 1740 tagattctgt agatcaaatt aaaaatatgc catgcttgga tttaagggaa tttggaaagg 1800 atgttaaacc ttggcatgtt gaaacaacag aagctgcccg caataatgaa aacacaggtt 1860 ttgatgctct gagccatgaa tgtacagcta agcctttgtt tcccagagtg gaggtgcagt 1920 cagaacaact cacggtggaa gagcagatta aaagaaacag gtgctacagt gacactgagt 1980 aaaatatcta tggccactga cagtccacac ttaggcactg agagatattg atgttctgaa 2040 ataagatttt atgaatttgg ataccctttt gaggaacttg atgtaaacat ggtgttcaga 2100 aatctcgtgt ctatctcaat gggatatttc ttgtattaca ccttgtcatt tttttcacaa 2160 tttatttaca tctacttttg tttgaactgg aatgaagaga tgaaacacta tggatatgtt 2220 ttccattcaa atggcacttt agcatattgt tctgttttcc tgtaaaacat catgggtgtg 2280 atttttatac tgctgctgct tgtcacaatt attataactt ctctgtaatt tcctctgaaa 2340 taaaattgaa tcacctgagg tgcaaaccaa aaaaaaaaa 2379 14 1904 DNA Homo sapiens misc_feature Incyte ID No 767447CT1 14 atgaatacaa atcgctcaga aagcattttg gtggcacaga aaggggatgt atttgtgttg 60 agatcttatt ttattttgta tttatttatc ttctttgact tgcacagcac tattgggggt 120 gggggaagca gggtagtggg agacgaaggc agaagcaaga gtcaaactca gaatgactga 180 gttgaattca ctgtctagtc agcaatgcct gcttctgagt ttggcccaga gagaaggtat 240 tgagtaagat tttaataact gtaaaaagta agctggataa gtaaaatcat gatggatcca 300 aagcacagtt tcttcatctc ctgataaaga aagtcaaatg cttgataaat tcagagtcac 360 agatgtgagc atagctatat tcttttaaac gagaggtaga gtgacctagc actaagcaaa 420 tgagctgaaa tgtcggaaac agagtccatc agcttatttg gccacacgat cccaaactag 480 ttttatcttg ggaaatggcc ctgtcctcag cattcccttc ttgtgctggt ggggccagtg 540 aagtcttgat cttatcagaa aaaggccaca ccaagtgcga gttttcccag gctgactttc 600 caggccctta tcaaatgaaa caacagaagc tcttcacagt tctgtgcccc atggccactc 660 cacagacaga caataccaag catcttagaa ctgtcataag ataggtcatg cctgaaatag 720 atcttgacca tatgagagtc ccagaaatca gcaaggcctg gacaaataga actaagagag 780 aggcagaggc aggaagctgc gggtctatct tgtaaagagt ttagcatcac tgtgagagtg 840 tgtgtctaaa attaaattaa actagaagca gcaggtgagt atttggtaag tacttctgtg 900 actcgcctca attcccactg gccaggggcc atctcaactg cacggtgaat caagatgctg 960 gtgtcatcct ccttggaaaa aggaaatgtt aactcatggt taaaactaag tacaatgatt 1020 cccaagggat cactttctta tttttttaaa tgacattaag gagaatctta agaaagcatc 1080 agagaaagac atgtgcatgt gaagcaccct gattctgatg ttaggaaaac ttaagcgaac 1140 aggacctgct gcacacagcc ccattgtctt ctatccattt ctctttatca ttcaaatcaa 1200 gcaacatgtg ccctcctcat caacacacat tcttcccctt tgtcagtatg catctcccag 1260 cttagtgtca ggatactttc gattcataat tatgtatgat ccaaagtgtg cataatttca 1320 tttaacgtta aagaaataga tccaattcct ttcttgcaac caaaaataaa taaaatacgt 1380 tgcctcaata taaggtttgg gctattctgt gtttctatag aagcaatctg tttttggtaa 1440 aatgtacttt taaggatcca gtcatctgaa gtattttatg tagagttaga gatttcacaa 1500 tattgactat acatatattt aaaatataaa ttatccagct gatgtttgaa tttgtcttac 1560 tttcctggcc acctcgttgt cctattttat aagctgggga gttaactagc ttaacaaaag 1620 atgcttagct tttgtaaaag aacaagtgtt tcattttaca aagacactcc aaatgatagt 1680 tacttgattt tctcgagacc tttaactatg gtgatgaata acaggacttg ctttcaagcc 1740 ttaataaatg taaaatgcct tttaatgaag atacagctga gtgttttcct catgaatctg 1800 aaccaattac caatttgtgt tccagtcttg attggtattg actgattcaa ataaagttgg 1860 tttattttca aatattaaaa aaaaaaaaaa aaaaaaaaaa aaaa 1904 15 968 DNA Homo sapiens misc_feature Incyte ID No 5449893CB1 15 gaatccaggg gaagggatgg aagaggaaga aaaacaagct tggagcagtc caacccagct 60 agggccctcc attccctcag ggacacccca cacccacccc acacactggg atgaaccctt 120 gcagaggaac aattcagatg gtcacacatt ccaggaccca aatccgtaaa cacaaagcat 180 gtccgtcagt gccagcacct ccccccggct aatcaagcag ctgtcccaga gggcaaaggg 240 tctctgcagc catctgcttt catcagggct gcagccccca ggcagcagta ctgggagccc 300 ctctcatctc cgagaataaa ctctgaagcc agcgaccctg cggacctgaa tcatcaggga 360 gcctgtcaga ggaggggcag tgactctgcg ggacaagcaa gcaggctata taagtttcag 420 aaggctgggc tccactcaga tcttttccag cagctgctgc ctgccagaga ggcgccttca 480 gagacccagc gcttacacaa tacccaccat gtcccaggct ggtgctcagg aagcccctat 540 caagaagaag cgcccccctg tgaaggagga ggacctgaag ggggcccgag gaaacctgac 600 caagaaccag gaaatcaagt ccaagaccta ccaggtcatg cgagagtgtg agcaagctgg 660 ctcggccgcc ccgtcggtgt tcagccgcac ccgcacaggt accgagactg tctttgagaa 720 gcccaaagcc ggacccacca agagtgtctt cggctgagaa gtgtgcgcca ctccccttgc 780 tgcccgaatg ctcggaaaca ggagccttac ccaggaactc ttttttatgc cagaacgctt 840 cctctcccct gctgtctctg gggctgccac cctcccccac agtccaggcc cttcagccaa 900 gggctctgca ccagcacctt ggaagcacca ataaagagga tgcccacgtg gccccagcaa 960 aaaaaaaa 968 16 1112 DNA Homo sapiens misc_feature Incyte ID No 2951269CT1 16 gaggcaagaa ttcggcacga agggtagacc tcacaggtgc ataaaatcat taataaagca 60 tgtagcactt gctaattggt gccttaagct tgaatctaat cagaattgca gactcgggtc 120 ctctgggaaa aaaacatgtc cgtctgtggc acgtgtgagt actaggccca ggggaagagt 180 ctgaaaattg aattcttttg tgtgtcctgt gtctcagaag agaactgaat gttcagagca 240 gcgtttgtaa gctattaaca ttcagtattt cgtgttgcaa ctagaacaca ttattagatt 300 tattcctgtt taattcataa tggtgcagaa taaaacacac acatctgatt tgatttcttt 360 ttcttttttt aagtttcata attgcttttt atggctagtg ttaatggcaa aaagtccttt 420 ccagggctcc ctgaataatc taccatacct gtatccatag caggtgatgc ttttttttat 480 ccccactttg aagacgtgtg tttctgtatt tacacataaa tcatactatt gtatattaaa 540 gacagcagtg gttgaaaaga atgtgaacac tgtagaagtt atgttggaaa aaaggagagt 600 aaattgtgtg attaatgggg aaggatattg gataatgtta taccccggac tatgaaaaaa 660 gctggtggta aatgggaaga atgtgaaatt ttaaactgct ctcaacgtag gaatcttggt 720 ggaaaagttc ctacctgagg tctgatatga ttcaattata gaatgcaatg agcttggcca 780 aggggacttt gaatccagcc aaggaaactt tgaatctcga cagctctgag aatcacattt 840 tcagtgcatt gaatatggag taaactattt agacaaggat tctgtgagac taggctactt 900 acctttaatt gccagcattt gtaaatgatt gtgcaatctt gtgtaatggt cttttatttt 960 gactgttttg gaaaaaaaat gttttattgt ttttttttcc cagtaaaaat tacttcaaag 1020 aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaggcg gccgcaagct tattcccttt 1080 agtgagggtt aattttagct tgcacttgcc gt 1112 17 1714 DNA Homo sapiens misc_feature Incyte ID No 282977CB1 17 ggaaagtgga agttggattc tgaaagatcg aggtgcccac aggaatttta tggtcgtcgg 60 attttgaaga cttgaactag actgggggtt ctccttgcat ttcttgcctg ttgcctatct 120 ttgtcctctc tcttccggct tcgagatgaa tgtgcagccc tgttctaggt gtgggtatgg 180 ggtttatcct gccgagaaga tcagctgtat agatcagata tggcataaag cctgttttca 240 ctgtgaagtt tgcaagatga tgctgtctgt taataacttt gtgagtcacc agaaaaagcc 300 gtactgtcac gcccataacc ctaagaacaa cactttcacc agtgtctatc acactccatt 360 aaacctaaat gtgaggacat ttccagaggc catcagtggg atccatgacc aagaagatgg 420 tgaacagtgt aaatcagttt ttcattggga catgaaatcc aaggataagg aaggtgcacc 480 taacaggcag ccactggcaa atgagagagc ctattggact ggatatgggg aagggaatgc 540 ttggtgccca ggagctctgc cagaccccga aattgtaagg atggttgagg ctcgaaagtc 600 tcttggtgag gaatatacag aagactatga gcaacccagg ggcaagggga gctttccagc 660 catgatcaca cctgcttatc aaagggccaa gaaagccaac cagctggcca gccaagtgga 720 gtataagaga gggcatgatg aacgcatctc caggttctcc acggtggcgg atactcctga 780 gctgctacgg agcaaggctg gggcacagct tcaaagtgat gtgagataca cagaggacta 840 tgaacaacaa agagggaaag gcagtttccc tgcgatgatc acacccgcct atcagatagc 900 caaaagagcc aatgagctgg caagtgatgt gaggtaccat caacaatatc aaaaagaaat 960 gaggggaatg gctggtccag ccattggagc tgagggcatc ttgacaaggg aatgtgcaga 1020 ccaatatggc catggttacc cggaggagta ttaggagcac aggggacagg gcagcttccc 1080 agctatgatc actccagcat atcagaacgc caagaaagct cacgaactcg ctagtgacat 1140 aaatacaggc cggacttcaa taagatgaaa ggcactgcac attatcactc gcttccagct 1200 caagacaact tggttctcaa acgggctcag agcgtaaaca aactcgtgag tgagaataaa 1260 tataaagaaa actaccagaa ccacatgaga ggccgctatg aaggagttgg tatggacaga 1320 cgcactctgc atgctatgaa agttggcagc ctggcaagca acgttgccta caaagctgat 1380 tataaacatg atattgtcga ctacaactac ccagccactc tcacgccttc ctatcaaaca 1440 gctatgaaac tggtgccctt gaaagatgcc aattataggc agagcatcga caagttgaag 1500 tacagctcgg tgactgacac cccacagatt gttcaagcca aaatcaatgc ccagcagctg 1560 agtcatgtga attaccgtgc tgactatgag aaaaataagt tgaattacac attgccccag 1620 gatgttcctc agctggtgaa ggccaaaacc aatgccaaac tcttcagtga ggttaagtat 1680 aaagaaggct gggagaagac aaaggggaaa ggat 1714 18 806 DNA Homo sapiens misc_feature Incyte ID No 3178454CB1 18 acttgtctca gtctggatca gactcaagtt gctctccaga atgcctctgg gaggaaggca 60 aagaagttat cccaactttc tttagtacca tgaacacaag ctttagtgac attgaacttc 120 tggaagacag tggcattccc acagaagcat tcttggcatc atgttgtgct gtggttccag 180 tattagacaa acttggccct acagtgtttg ctcctgttaa gatggatctt gttgaaaata 240 ttaagaaagt aaatcagaag tatataacca acaaagaaga gtttaccact ctccagaaga 300 tagtgctgca cgaagtggag gcggatgtag cccaggttag gaactcagcg actgaagccc 360 tcttgtggct gaagagaggt ctcaaatttt tgaagggatt tttgacagaa gtgaaaaatg 420 gggaaaagga tatccagaca gccctgaata acgcatatgg taaaacattg cggcaacacc 480 atggctgggt agttcgaggg gtttttgcgt tagctttaag ggcaactcca tcctatgaag 540 attttgtggc cgcgttaacc gtaaaggaag gtgaccaccg gaaagaagct ttcagtattg 600 ggatgcagag ggacctcagc ctttacctcc ctgccatgaa gaagcagatg gccatactgg 660 acgctttata agaggtccat gggctggaat ctgatgaggt tgtatgatgg ctgctgggca 720 gcacctccta acttcaggga ataaagtgct aaagtgtaaa aaaaaataaa aataaaaata 780 aataaataaa taaaattaaa aaaaat 806 19 555 DNA Homo sapiens misc_feature Incyte ID No 3563859CT1 19 gccagacacc tgagccgact ggtagtaggg gcagccgtgt ggcggggagc cggccgggcc 60 ttcctgctca tcgaggacct gactggctcc tgcttcgagc cactgcccca gggtctgctg 120 ctccacgagc tgcctgaccg ccgcagctgc ctggcagccg gccaccagtg gcgaggctac 180 accgtctcct cccacacctt cctgctcacc ttttgctgcc tgctcatggc agaggaagca 240 gctgtgttcg ccaagtacct ggcccatggg cttcctgccg gcgccccact gcgccttgtc 300 ttcctgctga acgtgctgct gctgggcctc tggaacttct tgctgctctg taccgtcatc 360 tatttccacc agtacactca caaggtggtg ggcgccgcag tgggcacctt tgcctggtac 420 ctcacctatg gcagctggta tcatcagccc tggtctccag ggagcccagg ccatgggctc 480 ttcccccgtc cccactccag ccgcaagcat aactgaaaga aataaaaacc atcgggcctg 540 aaaaaaaaaa aaaaa 555 20 1159 DNA Homo sapiens misc_feature Incyte ID No 985730CT1 20 taagatctac tcaaagtact tcaaacaaaa aataaataat tcattggctc atgtatcttg 60 gccacccagg gaaggtctga cattgttagt tagatccaga gtttcaaatg tcatcaccat 120 ggatgtgtct ttttctctct ctcatttccc ctccccatat cttgtctttt atttattata 180 ggtttgtctc attccctggc aggctctctc cctgtgatag gaaagagagt ccccagcagc 240 cccagggtga catagttgtt atagttcatt atggaataga agagagaaga gcattctcaa 300 taacccggca aagttcccag ggatgactct gatatgtcta tgtctcaggt cacatttcca 360 tctatgaacc aatcatattc agaggtggaa tgctaattgg ccaggcctgg gtcatatata 420 caagtctagg gaagaaatga gcttcatccc tgtccaattg acatggactg attaggggta 480 ttaatggaag aggtgtgcca ccacaaaaga atgtaccatg ggcagatcaa agaacatatt 540 ctgtatgtca ggcttggcac aaaagaatga cacaagtaat atgctgtaga tcagaacctc 600 tctgctaata ttgccttttt agcatggtta agatagctaa gatctagtac tgtcactcca 660 gtatgtccca attctaccta cgtttattga agggtcaaca gttctgatct cagcattggg 720 taaagggtgg gacattcaga tttacggtcc ttgataaaaa caatttacaa cgttccgttg 780 tgtaataaat gtaagtgtac atatgcctgg gacatcagct ggaaaaggga cagactatca 840 gagagttgca ctgttgcggt atgggccaaa tccaacataa tacccgctgt acctctagag 900 aactaaaacc ttaatttctc agatcttttc tgcactaatg gtctttacat acagcctaca 960 ttttaactaa ctcttgcatg ggcttgtttc acagcaggaa actatattca tcatatcctt 1020 attatgatag agaatgacaa cattcaaaag ggtgtggtgc ttctgaaaat atacacaata 1080 aatggcatga tttgaaaaaa aaaaaaaaaa aaagatcggc gcaagcttat tccctttagt 1140 gagggttaat tttagttga 1159 21 878 DNA Homo sapiens misc_feature Incyte ID No 3684987CT1 21 gtggcatcca ccattaaggt taagtgtggt gtgccctgtg agtctgaatg tctacttaag 60 aaccttaagt agacattaag aaccttaaga aggttttttg tttgtttttg tttttttgtt 120 gttgagatgg agccttgctc cgttgcccag gctggagagc agtggcgcaa tctcagctca 180 ctgcaacctc tgcctcccag gttcaagcaa ttctcctgtc tcagcctccc gagtagctgg 240 gactgcaggc gcctgccccc aagcccggct aatttttgtg tttttagtag aaatggggtt 300 tcaccttgtt ggtcaggctt gtctcaaact cctgacctca ggtgatccac ccacctcggc 360 ctcccaaagt gctgggatta caggcatgag ccaccatgcc tagcccacaa actcttacca 420 ttcttaaatg tatttatttc agttcctctt ccactactat attataacct accctggcag 480 tccttctcat ctgctgcaat atttcccatt ccttaagatc taacctatgc tgctccttct 540 ccatgaggct ttttctcatt aattcatgca cactgatctc tcccttctct gcattcctgt 600 catacatcat tatttcataa ttattttgca tgtgttgtac tttttctttt cagccacatt 660 cataagtctc tggggaaaga aattaggctt tcatgatttt gtatccttat cctacacccg 720 gcaaagtgct gagtatacag taaattctca aaggctttat gtcttcttca atcgaaaaat 780 ttacacttga agaaatttgt cttgtagcct atgaagtcaa acagtaccat taggaaacaa 840 taatcaagac tccatgacct aaccatgtta tattatta 878 22 667 DNA Homo sapiens misc_feature Incyte ID No 986166CT1 22 gcgttcagga gacagtcacg gtactcgttt ccagacagaa gtcatgagga acaagaggga 60 aggtgctttc ccgtgtgcag cgcttgggga gactcacaca gacagaggat ctggcatgac 120 agggaaagga ggaaatggct tctgttaatc tctccttcag cttctcccgc ccttcccatg 180 cactcttcct gtttcccttt ccagttctca cggtgactca aggaacaacg tgtgaaatga 240 aagacctcag gtgctgtatt ggctcttgac agctcttcag aagaaaatac ctcctgcctg 300 ttctgttcag tcctggtgca gcttccagga agccaaatga cccaccggct tacccacatc 360 gcaggaagct ttggagcaga gtcagtgact atgtgaacct gcctcaacct ctgctccctg 420 gttcagcatt tggcttggga aaaatgacac tatttcctgt ctcttaaaca ttatttcaag 480 gcacaggtct tccaccattc tgagaggcag ggggatcttt gagttctgcc aggagctggg 540 ggttaggggt aggggaatcc cgcccaaggg aaatgactag aatctttgtc aggctgtgga 600 acacaggcat tctggatagg tggctcccct gtggctctcc ctggaatcta catgcaaatc 660 cctgtat 667 23 1421 DNA Homo sapiens misc_feature Incyte ID No 1887508CT1 23 tgatcagtga tatcaaacat caggaatcag cctttatgta acataacagc tgtcctccta 60 tggtgaaagg ttcaaatgta gtgaaggtat aacctatatt gactgagatt tcccttttag 120 gtagtgcctt atctctatta ctagtgttaa aggaataagg aatctatgaa ggacagggag 180 cagctctggt ctgtcaatct cagccacctg tttgatatca cagagaagat actcggagga 240 ttgttggaat gtatatagtt tagtaagaag tgggtaagaa agagggtctt aattactgag 300 cacttattat gtattaggtt ctttgccaga tgtttttaca tatataaact catttcagaa 360 aacttattta aagtaaatgg ggccgggtat ggtggttcat gcctggaatc ctagcacttt 420 gggaggctga ggtaggagga ctgcttgagg ccgggagttg gagaccagcc tgagcaacat 480 agtgagaccc tgtctcaata ataataataa taataataat agtaataatg aagtaaatgg 540 gataaggaaa gaaggataat tatctttaaa ggttgattcc caccctccct ccccagttac 600 ttaaggaact aagtgagtac atctccagtt gcccatgaaa gcataagttt gttttcctca 660 gctgaggcaa gtggtagagt atacaggata acgaagtaac atgtaaaagg caggacgcac 720 ataaaggtgt acatggctat tgtttcacct ggagaaacca catgattggg acctgaaggt 780 ttactgactg actacagggg ctgattgtga agcacgagga accccatgtg tgtggagact 840 gtagggtgag agcacacaat tattagcatc atttctgagt gatctcacag attttttttc 900 ttgtgtttgt tttgcttttt gacaactgct tctcccacgt tccttgcaat tctattctct 960 caccttcact ttactatttg tattcgatgg accaggataa ttcaggcaag gttaccttgt 1020 aaacttgaat tggccacaca ccatgttgtc acccagctgg ctatgaagtg aataatggta 1080 ctgaaagtaa acctgaagac ctttctcaga tctattttaa gtctgagtct gaccaaccat 1140 ggaaaatatt cgacatgaat taatgtagag aactataaag catttatgac agctccaaga 1200 aaagtcatct actctatgca ggagatatgt ttagagacct ctcagaaaaa cttgcctggt 1260 ttgagggtac acagtaccat tttaatcttc tgaaaatatc tgtattcctg ctctttttct 1320 gctgtcactg tcaatctgct atatttttca ctatcctatt aaaatattac tgtctcctta 1380 aaaaaaaaaa aaaagggcgg ccgttcgcga tctagaacta g 1421 24 2630 DNA Homo sapiens misc_feature Incyte ID No 1006416CT1 24 aataaaggag ctccaaatgt cgttgggtgg ggaagcaaaa tgtagagaaa catttaaagc 60 acactgtaat aataaatgca attataaact atatggagga gggtgcagag gagggaatgt 120 gtctggtgtg tgatgtgtgt gtgtgcagtg ggggtatcac agagagtatg acatctgagt 180 tgagggtagc aggtgcctgg agtctcaggt ggctgctcac ccatctgtgc aggtgtctct 240 ggggctgctg gtctcacctg tggtctgcag tagacacaat tggctgagca ggatatgtga 300 tactgtgtgg ttggtgtgga gttttgaaga aggggctgtg tttgggccac gtaggctcta 360 ctcagagacc tgaaaccact tcagaatggt gcatatgtcg aaagagctgg ctgggggcct 420 tgcccaaacc aactgaggtc ttaaagtccg gggaaaaaaa gtctgggttc caactagaat 480 tctagaaata tttctagaac acacagagag ggaataagtc cctctatcac ccttattacc 540 aagccttgtg gttccctgtg attttagata atgtctgata tttttctggc tatttgccta 600 gtaggattta aaaaatattt tcaaagtgaa gctgagagag aatcttggaa acacacatac 660 ctgttgatca tgggccctgc agaattggcc cttgggggct ttatttggtt acatgtgcct 720 gggtggtctt taccagctta gactctatca tgggccccca tgaagctcca ttctcaatac 780 tgaataatta ttacttccct tgttgagttt ctttttctgt catgccctgg gggcttctgc 840 tcttctcacc agaaagaaca tttgaatctg gattcttgta cacctgggtt agaccctgtt 900 cagaggtgtg gccaatttat cccgatctcc tggaaggctg ttgtgatttc catctaagaa 960 atgagggtct tgagaatcaa ccagtcccaa gattagcctg ttatcctgtt atctactgag 1020 acctcaaatt tctcaccaat gttttgggag atcctggaaa agatcccttc agtttggggt 1080 gtcaccaaga cttctacaca acccaggact accattgacc tcagagctgt accccacatc 1140 ttgaagtaaa ttgatcccac caggtcccac gtttgttatc tctgcctaaa tgttagcttc 1200 tccatcctca ccacatgatg acctgctgtg tccctctgag cactacccag tggctgaaaa 1260 ctctgcaaat gggccacact tttgcaaaat acttgtatct gacacttagg tcttgtttga 1320 agaatttcct ttctggaagg ttttacaaga agactgatag tctttcaagc ccccacatca 1380 caggcttagg gacggcacta actttctccc agggatctaa ctggctagtt caaattatca 1440 ctcttttacc ttcatataaa atgtctcccc caaacctttt tcccttcttt gtcattgtta 1500 tctgctaagc cactggtcat ttccccatat tcgtagtctt tttttccatc ctatctttct 1560 aatatttgtt gtctttaaca aactgtgttc tgtgtctgtg ctcctccttc cctctcagac 1620 cactggaatg caagtccttc ttccctttgg aatgtactct ggatcccttc ccctgctttg 1680 acccccagac tttgctccat ctattattgc ttctccatcc tggatccttg acatttgtca 1740 ccccactggc cttctcaggt gcaatcagta aaaatgctga gaactcttgg atcttaatct 1800 tcatgactga gtttttttta gttgtatagt tatcatctgc ctttcttcac tttgcatttc 1860 ttcttgaatc cattgcagat tgacttccac tcccactcct tcactaaaag ggctcttacc 1920 aagatcaaat ctaatgggta cattttagtt cctatgtgat ttggcctttc gatgtcaatc 1980 atcactccca gccattgatt ttggtgaccc acttccctgt gatgatcttc tgatctagtt 2040 tctcaggttc cttcgctggt cctttttctt tccctgcccc tgacatattg acatttcctg 2100 gagttggttt tgtccttgat tcattctcat gtcattctgc acacagtctc tgcatgaact 2160 caggcagacc cttcatttaa tgaccacctt agggctgatg attctcaaat ctgtattccc 2220 cgatcttgca tttgagctcc agccccactc atcctctcgg atgttctgca ggcccagcaa 2280 actcatcatg tccaaagtga aactttttct ctttcctgtc tcctctcctc tgatctgttc 2340 tttcttggaa caccacccaa gaacgtcacc tcctccatca gattgtgagc tcctggaggg 2400 caggagctgt gtccttctat tcatcttcct atccccagaa ccttgcacag atcctggaat 2460 gtggtaggtg ctcagtaaat gtgtgttgaa taaatgaatg aatgaatgaa caaatgaatg 2520 aatttgctta cttcaaggca aaagaaccat gaaactgtat tttgagtttc tatgttatag 2580 cagtcagcaa atcctattaa atactttgtg tttccaaaaa aaaaaaaaaa 2630 25 1039 DNA Homo sapiens misc_feature Incyte ID No 975169CT1 25 gttgacacgt tgtatgccat cctggatgag aagaaaagtg agttgctgca gcggatcacg 60 caggagcagg agaaaaagct tagcttcatc gaggccctca tccagcagta ccaggagcag 120 ctggacaagt ccacaaagct ggtggaaact gccatccagt ccctggacga gcctggggga 180 gccaccttcc tcttgactgc caagcaactc atcaaaagca ttgtggaagc ttccaagggc 240 tgccagctgg ggaagacaga gcagggcttt gagaacatgg acttctttac tttggattta 300 gagcacatag cagacgccct gagagccatt gactttggga cagatgagga agaggaagaa 360 ttcattgaag aagaagatca ggaagaggaa gagtccacag aagggaagga agaaggacac 420 cagtaaggag ctggatgaat gagaggcccc cagatgcaga gagactggag agggtgggga 480 ggggcccagc ggcccttggt gacaggccca gggtgggagg ggtcggggcc cctggagggg 540 caatggggag gtgatgtctt ctctctgctc agagagcagg gactagggta ggaccctcac 600 cgctgcgtcc agcagacact gaaccagaat tggaaacgtg cttgaaacaa tcacacagga 660 cacttttcta cattggtgca aaatggaata ttttgtacat ttttaaaatg tgatttttgt 720 atatacttgt atatgtatgc caatttggtg ctttttgtaa aggaactttt gtataataat 780 gcctggtcat tgggtgacct gcgattgtca gaaagagggg aaggaagcca ggttgataca 840 gctgcccact tcctttcctg agcaggagga tggggtagca ctcacaggga cgatgtgctg 900 tatttcagtg tctatcccag acatacgggg tggtaactga gtttgtgtta tatgttgttt 960 taataaatgc acaatgctct cttcctgttc ttcaaaggaa aaaaaaaaaa acaaaaggga 1020 aaaaagggag agaaaagag 1039 26 1057 DNA Homo sapiens misc_feature Incyte ID No 4152861CB1 26 ggagtcgggt tacaccactt gtgtctgagt tcacgcagca tgttcctctg tcagggattc 60 cgcaaatatc tccctgaggt aaaaaaggaa agtgtgctgc gctccagcac ccagagcagt 120 gagcccagtc ccgagtcccg gagagagctc cagcaatagg ggccatgtcg ccatagcccc 180 agcctctcgg tccgcagcct cagcagcgtc ccagccggct ggcttcatgc tgcggtgcag 240 ctgcaccatg ttcctgggtt gagggggcaa tcgggcacgc tcctccccat gggttgccca 300 tcatgtctaa tggatatcgc actctgtccc agcacctcaa tgacctgaag aaggagaact 360 tcagcctcaa gctgcgcatc tacttcctgg aggagcgcat gcaacagaag tatgaggcca 420 gccgggagga catctacaag cggaacactg agctgaaggt tgaagtggag agcttgaaac 480 gagaactcca ggacaagaaa cagcatctgg ataaaacatg ggctgatgtg gagaatctca 540 acagtcagaa tgaagctgag ctccgacgcc agtttgagga gcgacagcag gagacggagc 600 atgtttatga gctcttggag aataagatgc agcttctgca ggaggaatcc aggctagcaa 660 agaatgaagc tgcgcggatg gcagctctgg tggaagcaga gaaggagtgt aacctggagc 720 tctcagagaa actgaaggga gtcaccaaaa actgggaaga tgtaccagga gaccaggtca 780 agcccgacca atacactgag gccctggccc agagggacaa gatctaaaaa aaataatgct 840 gggaagtcct aaccacatca agaatgcctc agatcagtga cccaaggaac cttccagaat 900 ggatgaaata gacccaaagc tgaattcacc taattttagg gccaaaaacc caaaaaacaa 960 aacaagacca aaaaaatctt cagatactgg gagaacaaat ctcaattgct caattgtatc 1020 ttatgaaaac aatttttcaa aataaaacaa gagatat 1057 27 1363 DNA Homo sapiens misc_feature Incyte ID No 986464CT1 27 gaaatcacac agaggccaga ggtcacacag cctcaactgc cccttccacc aggaggcagg 60 agacatcaag agagtatttg tgccctcctc gggttttacc ttccagccga gattctccct 120 cctccccaac atttatctcc atccagtcgg ccacaaggaa gcctctagag actcccagct 180 ttaagggcaa ccctgatgtc tcagtgaaaa gcacacaact ggctcaggac ataggccagg 240 ccctgctcca ccagaaaggt gtccaagaca aaactgggaa gaaggacatc acccagtgct 300 ctgtgcaacc tgaacctgcc cctccctcag ccagtcccct gcccagaggg tggcaaaaga 360 gtgttctgga gctacagacg gggccaggga gctcacaaca ctatggagcc atgagaaccg 420 tgactgaaca gtatgaggag gtggaccagt ttgggaacac agtcctcatg tcttccacca 480 cagtcaccga gcaggcagag ccacccagga acccaggctc ccacctcggg ctccacgcct 540 cccccttgct gaggcagttc ctgcacagcc cagctgggtt cagcagtgac ctgacagaag 600 ctgagacggt gcaggtgtcc tgcagctact cccagccagc tgcccagtga ggcccaccgc 660 ctcccaccac acctgccacc tgttcctggc ctccactgcc ccaggactga agtgggtacc 720 tgcctcctgt acactggagc aaggaccaag aggaaatggc atcttcagag gattactgtg 780 ggccatttcc ctttcgcagt tctttcaata ggcccagttc ttccaaatgg aaaaagaaag 840 gtctggaaga ggcccacaga gttgcacagg cgtgggggta ggatgggggc tcccagctgc 900 ttgtggagga tgtaatatat acagacacac acatgttttt cacacaggcc tggcccacgc 960 atcgacatgt gtgaatttgc acaccactgc ctgaattgga gccccccaga gtgtccctct 1020 acccagagtt tttatttctt taattagtct gagtgttccc agccatctgc tccttaatcc 1080 ctggagagga acagagccaa ctggacacag cgttggtctc tgtttggaat cactgtgagg 1140 tctccagaag gacctggccg ccagcccctt catcaccatc tccatcattc agctggtcat 1200 ctggtggccc aaaggtcacc caaagagtca gcaatcagca tgtccctaga agccaaatgc 1260 actgcctttc tctgtcccca tgactgtccc ccactctgca ccccaaatgg gaagcatacg 1320 gtctgaataa atccaagttt tattctctaa aaaaaaaaaa aaa 1363 28 1513 DNA Homo sapiens misc_feature Incyte ID No 118472CT1 28 cttcaacatg cccctcacta tctcccggat cacaccaggc agcaaggcag cccagtccca 60 gctcagccag ggtgacctcg tggtggccat tgacggcgtc aacacagaca ccatgaccca 120 cctggaagcc cagaacaaga tcaagtctgc cagctacaac ttgagcctca ccctgcagaa 180 atcaaagcgt cccattccca tctccacgac agcacctcca gtccagaccc ctctgccggt 240 gatccctcac cagaaggtgg tagtcaactc tccagccaac gccgactacc aggaacgctt 300 caaccccagt gccctgaagg actcggccct gtccacccac aagcccatcg aggtgaaggg 360 gctgggcggc aaggccacca tcatccatgc gcagtacaac acgcccatca gcatgtattc 420 ccaggatgcc atcatggatg ccatcgctgg gcaggcccaa gcccaaggca gtgacttcag 480 tgggagcctc cctattaagg accttgccgt agacagcgcc tctcccgtct accaggctgt 540 gattaagagc cagaacaagc cagaagatga ggctgacgag tgggcacgcc gttcctccaa 600 cctgcagtct cgctccttcc gcatcctggc ccagatgacg gggacagaat tcatgcaaga 660 ccctgatgaa gaagctctgc gaaggtcaag ggaaaggttt gaaacggaac gtaacagccc 720 acgttttgcc aaattgcgca actggcacca tggcctttca gcccaaatcc ttaatgttaa 780 aagctaaaag gctgcctgga atccccccac cccaacaggc tggactccct ccatccttac 840 ccccacacag atctggcatg tgagccccac ggtgatgctt gacaatgtat aactctgctg 900 ggggcacctc tgatggccaa ccgcagcatt tctgtcctct gcccacccca gagctgatgc 960 tggggcccag ccccctgcag ctctgtaccc accaaacctc cccagggcaa ccctcgccac 1020 cccccaaata gcccgtagcc caatcccctg ccctctgcac agggccttag ctgtagacca 1080 gagagggcag gaggggtttg ctggcataac accccagaac caagggaaat ggatgggccg 1140 ctgctcagtt tcccaccatc ctcagctcct ggcctcatcc cctcctagaa tgagtcaccc 1200 gtagatcagg gtctggggaa gaggctgatc cctggcgctg cccggctccc tcgctgccct 1260 ctggagctca gggcagcccg gaatagggct ctttgaagag gaagtagaag ccccagggta 1320 atgaggcaga gacccctcct ggcagtggtg aggtgggggc atgcaccctc ctttctgtac 1380 cgtgtgtgct ggctccatag ttctctcttc tgtacatata agcatgcttg ttctgaaata 1440 aagaagattt gaagtgaacc acaaaaaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaataa 1500 aaaaaaaaaa aaa 1513 29 627 DNA Homo sapiens misc_feature Incyte ID No 1314633CT1 29 gcctgtgtga gcctgaagac ctttctgtcc tggcgacccc tcagaagggc tgcactggat 60 cttgtctgcc cggggagcgc acctatccat tggagggaag agcctcctgc gggtagagga 120 tggccagcta ctcagcaaac tggacttgag ggggcctggg cagctggagc cctgctctga 180 ggaagaagca cattccctga agcgtctgga agatcagagc cctgggccac caagggggtg 240 gcctgcagga agagcccctt cacggagaaa ccttgctcag aatccctgcg ggtgccagtg 300 gagccgcttt tcgcctttgg ggcattctgg actcagcttg ggctgctgct cccgacccct 360 acccccagcc ccatgcccgc gcttcccctg ctgtgtgtag tgggagatct ctctgtgcct 420 ggcagcccct gcagaccctg ggagggagct caggctgagc caggcactgc aggggatctg 480 ggaaagccaa gatgggcaag gaaacccttc tatggccagg agtggtggct catgcctgta 540 atcccaacac tgtgagaggc caaggcagaa ggatcagctt gaggtcagga gttcaagacc 600 aaggggggca gcatcgtgaa gagaagg 627 30 1606 DNA Homo sapiens misc_feature Incyte ID No 1997439CT1 30 ctcgtagact cgcattgact taattttttt aaatcttatt gcatattttg actagataat 60 aaatgcatat ggttaaaaaa ttcacatggt tcaaaaaagt acacctccca ctcatcttcc 120 atgtgatatt tcctttctgc ttagcaattc tgtatttatc ttgctaaaca tgaatgacag 180 ttgtttgctg aaattacatt aaatgtgacg taataaaatc attgtaagta tacatttttt 240 aactttaata atttttaatg tcttaatgaa gagtatgaag agtagtagta ctgctcttca 300 aagtactact actttacctt accttttact gttttgttaa gaaaattagg ccgggcgcag 360 tggctcacgc cggtaatccc agcactttgg gaggccgagg cgggcggatc acgaggtcag 420 gagatcgaga ccatcctggc taacacggtg aaaccccatt tccactaaaa atacaaaaaa 480 ttagctgggc gtggtggcga gcgcctgtag tcccagctac tcgggaggct gaggcaggag 540 aatggcatga acctggaagg cggagcttgc agtgagctga gattgcgcca ctgcactcca 600 gcctgggcga cggagcgaga ctctgtctca aaacaaacaa acaaacaaaa gacccaatct 660 gagtcttatc gttgtactga tagaagggtc agatatcccc acatggagtt gagtgggaga 720 aagagattca ctagagaata actccttaga gaccaatgtc tgtagcaggt gtacagcatc 780 ttgtgaaagt tatggagcat gaaaagactg aagggccagg acagtttgca tgggctgagt 840 tataccagct agaccaggaa tagaacaaag aattctatac ctcaggattt caaaaagtta 900 gcaacttgag aggccagtgc tgagcaaccc agtacccagg aaatgaaaaa aaaaaagaaa 960 attccctccg agaatgaaca aatcattggc ttcattgcct catgagcttg agagaaagga 1020 gaagagagcc agagtgtggc aagtgaggcc aaaatcagaa gcatggcaga aatgagtgta 1080 agtgattgag ccacagacag aagtgtggcg agggacaatg ccatattggg agaaggtaaa 1140 gttgagtaac aagaaaccaa ccgtgtgtga gagggggatt ggaaaaaaat ttgagggaga 1200 agaatgttag aatggaaggg aatgatggtg gaagggaggt gtgagggtgt gtgctgagtg 1260 ttgaaagaac ggttggtgtc tgtgtgattt tccttgagtc tgttcttcag tgtgtcttct 1320 gcagcttgcc atgactgcct gggaaagagt agggaaatac ccagagccaa aacctccttt 1380 cagtcccacc ccatccctca aaaccccagc tattgcttct tttcagcttc aggtcctgat 1440 ctccaatctt agtatggact cccttctcac caagaccacc accagctacg tttgctgtgt 1500 aatctggaaa gtgataattt cctttgcttg ttgggtgtga gtcacaatac tttggtttgt 1560 gcacaagaat aaatttatgc cccatacctt caaaaaaaaa aaaaaa 1606 31 2184 DNA Homo sapiens misc_feature Incyte ID No 2638878CT1 31 gccaaatgga ttgagtgatg agcagacatg tttaagggtc taagtctcaa gaatctgtta 60 tgtgtgtttg ctgcggtggg agggggtgct tgtatttatc ttatttccag tcactataag 120 gttgtacaca aactaattta aagtttactt aataatggta tctttaaaat aattgacaca 180 attgcaaaat gaattcctgg cttcagttag ctattatttt tttaatgaca acatagactg 240 tgctctaagt ttaaaagatg gggaagctta tataaaagtg acccttttgc atcatatggg 300 tatctaaact taatttaccc aataagttga tgcttaatga ttttatttta tttttgtcta 360 tttctatttt agttgtggct ttgctctaag aatgggtaat agttgtacta cagactgcta 420 taaatttctt gtgatactct tttagagctc aaaatatctc tgagctttag acatggtaag 480 gtggagagta aatgcttgat aaatctttaa gatatgtctt gaatgataat taggacattc 540 agtccagtgg aaatacacca ttcaattagt caggtctggt gaatcgtttg tttaaaatat 600 tagcaaatga gatgtggaat tctgaaattt ctccagactg tgtcttaata aaaatgtcac 660 ctgggtgaaa ttttagatca atcactaaat ttgggtgaca aatataaaaa tattttcatt 720 tcactttaat acattctttc tgtgaagtaa aatgtttttc tttctcataa tggcaaaata 780 tgaatgccat caaagtttaa ggaattcatt ttagccttaa atgccttcgt gagatgtctt 840 acttgtattt taggtaactg gtcatcagtg ccaatgacat ggataacaat ttttaatcta 900 ctcgacagtg catccctggg aatgactgtt atgtttttgt catattcctg gtaatataaa 960 tactcgtgtt ctttactaca ttgtttttat caactctaaa agtcatgcct ctgtgacctt 1020 tatcatgttt acaattgcaa ctgaacttat gacaaattaa ctcaggaaat aaattgagtt 1080 atcctttcta gcattgtaat taccatcagc aaggcctgag atagccagag ccaatactag 1140 ccaagtgatt tattttcaag gattgccact aactacggtt ctttaggacc aagatataaa 1200 acagtcacta aaaatcatta ggctaggtat cagtaataca ttcattacta ataatgcatt 1260 tttggagact tttgtgaaag aagttggtct ctgccaaaag ctggtggacc acattcacac 1320 cacgaaagcc agtgtcacat gaaccagatt aatgactctc tttatggggt atgtgggaca 1380 tcctggaagt gtataatttc aggaatgacc agacaatacc atcttgcaaa gccccttcag 1440 gtgacaatct aaacttgtgg gtaggagagt gcataaagtt tattgctcaa ctgctcctcc 1500 agcctgctga atttactgag taaagaaata gcaaatatga tagatgtttt agatttcata 1560 gaacagaatg gtttgtccat taattctttc attcaatgac tgtttattga atacctactc 1620 ttttagggcg ctgtgttagg tgctgtattg tacaagaaaa atataataaa ttagattccc 1680 agcgctattc tgacatagtg aatgaccttg aaaaatttac taaacatact atgtttgttt 1740 ctccatgagt aaaataggga tatagggaca aacagtctaa tatctcatag aaataccatg 1800 gagacaaata aaatatttta atataaatat gatattaaag taaatttctg aagtaatact 1860 tttgggtatg gcactagttt ttcctctgac tattttactg tttctttcac tctcaatata 1920 aaaactattt gataagataa aacgatatat tttattgtaa ttagaattta gacaaatcag 1980 ctataatgta aaaatgttaa taataattac gttttatctg attaaagtta caatgatcat 2040 agcactttaa aaatattatc tgaactgtca tttgtttata tattaccgtc taataaaata 2100 gttatagatc ttccaagttt gatgccttac attttaaaag gaaaagataa atggttgatt 2160 aagaaaaaaa aaaaaaaaaa aaaa 2184 32 1833 DNA Homo sapiens misc_feature Incyte ID No 3795510CT1 32 cgggcagtgc aagctaaaat taaccctcac taaagggaat aagcttgggc cgccattttt 60 tttttttttt tttttttttg ctctttagaa gaggttatat ttttattatc cttattttgg 120 agaacttttc cttataaaat tttttttcca gattccttat gaactcaagt tagtgttaaa 180 gctttggatt ccactgttaa cagtttatgt aaaaacactt aacaaattgc catttatatg 240 ccaaactata gctcaagaac actctgtttt agaaaaatta cgcattagat caggaagcct 300 catatatatg tgcctctggg acttcatttg cagtcacatt tagccagaaa agcaatgact 360 tctatattcc ttatggaaac caatgtaaca taaattaatg ttctaaatat agaaattaag 420 agttcataaa gagactgagg ttgcatgtaa aagagttatg gtttgagaca gtctaaaaat 480 actatgttaa tttcaaggat cttatttcca atgttttgtt taaaaaatta taaatacttt 540 tgagctcttg ctttgcattt caatcgcaaa cccactcaga tacgggaact gtttaaattc 600 atatatggac aaataggttt cagtgatgca atactttaaa attctgccat ctccttgtgt 660 ttttctttct aggtgagtgg actgccagct cctgatgtgt catggtatct aaatggaaga 720 acagttcaat cagatgattt gcacaaaatg atagtgtctg agaagggtct tcattcactc 780 atctttgaag tagtcagagc ttcagatgca ggggcttatg catgtgttgc caagaataga 840 gcaggagaag ccaccttcac tgtgcagctg gatgtccttg caaaagaaca taaaagagca 900 ccaatgttta tctacaaacc acagagcaaa aaagttttag agggagattc agtgaaacta 960 gaatgccaga tctcggctat acctccacca aagcttttct ggaaaagaaa taatgaaatg 1020 gtacaattca acactgaccg aataagctta tatcaagata acactggaag agttacttta 1080 ctgataaaag atgtaaacaa gaaagatgct gggtggtata ctgtgtcagc agttaatgaa 1140 gctggagtga ctacatgtaa cacaagatta gacgttacgg cacgtccaaa ccaaactctt 1200 ccagctccta agcagttacg ggttcgacca acattcagca aatatttagc acttaatggg 1260 aaaggtttga atgtaaaaca agcttttaac ccagaaggag aatttcagcg tttggcagct 1320 caatctggac tctatgaaag tgaagaactt taataacttt accaacattg gaaaacagcc 1380 aactacacca ttagtaatat atttgattac atttttttga aattaatcca tagctgtatt 1440 aacagattat ggttttaatt aggtaatata gttaatatat atttataata ttatttatcc 1500 tttgactctt gcacattcta tgtacccctc cgatttgtga agcctacagg aaatctgggt 1560 atatggattt gtaactgcag aagactatct taaaatacag gattttaaca tttaagtcat 1620 gcacatttaa caattacagg ttataaatta gtatcaactt tttaaacaca tctaatgctt 1680 gtaataacgt ttactggtac tgctttctaa atactgtttt acccgttttc tcttgtagga 1740 atactaacat ggtatagatt atctgagtgt tccacagttg tatgtcaaaa gaaaataaaa 1800 ttcaaatatt taaaacggaa aaaaaaaaaa aaa 1833 33 1859 DNA Homo sapiens misc_feature Incyte ID No 1413537CT1 33 cttctctttc ctgagcctct ttagagcagc acttacagga ttgcctctgt aaagccttat 60 tcctgtccca gaaaaggtaa tccaaaaagt ctctagtatc cactaaaagg taacccaaaa 120 atctctagta tccactggct ttctccagtg tggaagcttt cccctccacc tcccatagat 180 cactggaaag gacccgaggc ctcggttcta atccctggct tatcactaac tgctgtgtgg 240 ctttggcttg tcccttagtc tctgtgagac tgctgcaccc tcatctgtca aagatggaac 300 tggacttagt tgagctctga ggtccctgtg gacttggccc ctccacaccc tcattatggc 360 aactggacat aaacttaaca gagggcttcc cagcaaaatg tcctcttctt cctacaaaca 420 ggctgtttct atatgtgcat gtttcatgct aagcacttct ttcttgggtg gagatggcaa 480 aggcctcttt ctgctgagac aaagtgattt ggagagtcac ctggcccctg aagggggagt 540 ggtaggatcc agccacccag tgtgcagtga attggagcag ggatctcagc acacagggag 600 gtggggaggc tccccctaac ctcgggcacc tgttgctcct ccagactgca gcgcatgctc 660 ttagctcatc ctcttaactg gctctcaccg tgctcctggc tttggtcacc acgtagctct 720 cactccagct tcaggtagcc atcagtagga cctggcaata tacactgatt tggtttgttt 780 tatgtttgtc tgcaggtgaa atccctaagg gctctgccgt gtactccagc cttgtgaccc 840 ttgccttcca ggaaccatgc aagaagcgca gccaccagaa gtccttaaaa cagcaggaaa 900 ggtgagcctg tccccctttt gtgcagctac ctatctgctg aggagcatct gggcctcatt 960 cctccaagtc cactggaggg tccagaagag ggagtcagag atgtatcctg gtggagctgg 1020 gagaaaggca gaaagccttt gtgacagcta tggaataccg ttagccaagg tccacttggc 1080 ccagcactaa gcaaaagatg cgtagtttgc acagaaggtt ttgtgatact gcctctcaac 1140 agccccagca gcttgggaac tagcaagagc acatttcttg cctcatcagc tgtcctgaga 1200 tggaaaactc agtggatata ggaccctgat tccgatgaaa ggggcacgtg gtcccaatgc 1260 tggagctcct ctggcaggtt ctaaaagcac actacggagc agcggtgccc tgccggacac 1320 tgctggcggg ggctcagtga gcactactca cagatccaca cctgaccctg ttgggtcgag 1380 tcaggctggg ctttggtctg cactgtagca cctgtgttct ttgagttcac atcatgaatg 1440 tggtgatttc ccagatacca tctcaggctt aacctagcac atcctatttc ttttcttcta 1500 tgatatccaa attggactga cctcacttca aagttgctgt cccattttgt caccctatct 1560 tatctcgggg aaattgcaga ctgatggcca gaccaactct gttgaaattc ttgcatagag 1620 caaacctgtg ctcattttta agtggcatgg gagaggcccc aagcctagta aagcctagtc 1680 tgtgtcttca cagtgctggt agaatgtgtt tgtgtgtata aatatatgat atagatttat 1740 atatgttgct aacgccacat attgaaggcc aacataactg gtggacaggg tgggtgacag 1800 aaaatgaaag tctttttggt gattgtttaa gcaagatgtg tataaagaaa taaatagtt 1859 34 2125 DNA Homo sapiens misc_feature Incyte ID No 1623157CT1 34 tgtgtaaaca ataacaagaa gacatgaagg atttatttgg ttatcaactg cccatggagg 60 aggctcttga tgatcccagg tctcctcgac ctccatacac cacacaggca tttgtaagca 120 cagtttccac aagcaccttg taggaatatg gataagatta gaccagcccc tctctgtcca 180 ctgggtttat ttcttgaaga agatgcagat ctggtttttc caatgtgcca cagtctttcc 240 ttatcctctc catgctgagc ttgacaacac tctgggaatg aggaacaaga ctttttctaa 300 aaagatagtg gaagttcaag ggatgtacct cgttttcagg ttcatccatc tccagtggaa 360 tgttttcaat aaaagatgaa gaaaatgtgt gtgatcttta ataacacatc cctatagaaa 420 gtggataaaa gatataccaa aactgtaata cagatatata caaatatagg tgcctttttg 480 attactcttg tttgtctagt atggtcttgg aaagaaaacc aagcaagcaa gttgctgcct 540 attctatagt aatattttat tacacatgat tgatattttt gtggtaggga agtgggatgc 600 tcctcagata ttaaaggtgt tagctgattg tattttatct ctaaagattt agaactttag 660 aaaatgccga cttcttccat ctatttctga aaggttcttt gtggatttat atagagttga 720 gctatataaa cattaacttt agatttggga tttaaaatgc ctattgtaag atagaataat 780 tgtgaggctg gattcactac acaagatgaa cttcacttca taaattaatt ataccttagc 840 gatttgcttc tgataatcta aaagtggcta gattgtggtt gttttggtta aggtgatatg 900 gaggtgggag agcttttagt taagtaagaa gctatgtaaa ctgacaagga tgctaaaata 960 aaagtctctg aagtattcca tgccttttgg accctttcct cgcaactaac tgtcaactgt 1020 tgatcaaaaa agtcaaggca ttgtatgttg cttctgtggt tattattctg tgatgcttag 1080 actacttgaa cccataaact tggaagaatc tttgagcaaa ttttctcagt tgtctgtatg 1140 acttcagtat attcctggga atgccatagg attttttgtg cttgatacat ggtatccagt 1200 ttgcatagta tcacttcttt gtaatccagt tgctgttaag aatgatgtac tttaaaggaa 1260 aagagaaaac tgcatcacag tcccattctc cagtgtccat gcaatgaatt gctgagcatt 1320 taggaagcag caccaagtct attacaggca tggtgtgaaa cttgatgttt gacctgtgat 1380 caaaattgaa ccattgtaca gtttggcttc tgtttgcttc aaaatatgta gaattgtggt 1440 tgatgattaa tttgcgagac taactttgag agtgtaacag ttttgaagaa aacattgaat 1500 gttttgcaaa tgaaggggct tcacggaatg ttacaatgtt actaatataa tttggctttt 1560 gttatgcaaa ttgttaacac cagctattaa aatatatttt agtagaaatg ctttaattca 1620 tatttttttc ctctacactg tgaatcttta agccttggtg gactagagca acatcgtgct 1680 gcccaaagga ctaacctatg caaactagtt cacattttag tggatgtcgc agttaatgtg 1740 taataagaca ttatttcccc tgcataatgt acaacagcat tgaaatgaca cattaagcct 1800 agcatcacat tgtatagtac agtcactcac aaacccttca aggctaccct aatcattaac 1860 attaatattt gtttaaaagc aaatcaccga tttatctatt gaaactactt aaatgacggc 1920 aaaccaggaa tgacagatgg ctgtgtcagc aatggcttta atgtgttccc tgcaagtggt 1980 ctcctatgat agaactgcgt tctcaaatgc actctcttca gggtcttaat attctgtgtt 2040 ttctctctgt atttgtaaaa cattataaca cattaatttc ctatctctac acatttggtt 2100 tgcttaaata aatgcaggat ataaa 2125 35 1686 DNA Homo sapiens misc_feature Incyte ID No 3009303CB1 35 tctgactgcc agcaccttac agagaagaga ccatcaccac tgtggtgaag agcccacgtg 60 gccaacgacg gtcccccagc aagtccccct cccgctcacc ttcccgctgc tctgccagcc 120 cgctgaggcc aggcctactg gcccccgacc tgctgtacct gccaggtgct ggccagcccc 180 gcaggccgga ggcagaacca ggccagaagc ccgtggtgcc cacactgtat gtgacggagg 240 ccgaggccca ctctccagct ctgcccggac tctcggggcc ccagcccaag tgggtggagg 300 tggaggagac cattgaagtc cgggtgaaga agatgggccc gcaggtgtgt ctcccaccac 360 agaggtgccc aggagctcat cggggcatct cttcacactg cccggtgcga cccccggagg 420 gaccccaatt ccaacaactc caacaacaag ctgctggccc aggaggcctg ggcccagggc 480 acagccatgg tcggcgtcag agagcccctt gtcttccgcg tggatgccag aggcagtgtg 540 gactgggctg cttctggcat gggcagcctg gaggaggagg gcaccatgga ggaggcggga 600 gaggaagagg gggaagacgg agacgccttt gtgacggagg agtcccagga cacacacagc 660 cttggggatc gtgaccccaa gatcctcacg cacaacggcc gcatgctgac actggctgac 720 ctggaagatt acgtgcctgg ggaaggggag accttccact gtggtggccc tgggcctggc 780 gcccctgatg accctccctg cgaggtctcg gtgatccaga gagagatcgg ggagcccacg 840 gtggggcagc ctgtgctgct cagcgtgggg catgcactgg gtccccgagg ccctctcggc 900 ctctttaggc ctgagccccg tggggcgtca ccaccgggac cccaggtccg tagccttgag 960 ggcacctcct tcctcttgcg ggaggccccg gctcggcctg tgggcagtgc tccctggacg 1020 cagtctttct gcacccgcat ccggcgttct gcggacagtg gccagagcag cttcaccaca 1080 gagctttcca cccagaccgt caacttcggg acagtggggg agacggtcac ccttcacatc 1140 tgcccagaca gggatgggga tgaggcggca cagccctgat gctgctgcca tggtggcttg 1200 gggcagcggg gagaaaggag tgtccttgag gcctaggacg ctgcccggcc tcagcagcag 1260 ccctgggagc ctcctgaggg ccctccctgt ccctggccac gggcccttct tacctcactc 1320 aacttcagcc aggaggactg ggtggtgctt gcaatgttgg aatgaccggc tcaaagacct 1380 cagctctggg ctgtttcctg tcagcctggc aggagcctca ggactgtgga cgaaggatgt 1440 ggccttgggc atttgtcctg ttcccacatg ggcctggtcc ctccctcctg gccccagcca 1500 cagctgccag gcctgacatg gccttgcctc tcctgcagtc ttggtgactg agacccttgg 1560 gtggcgcttc ccagctctgc aggccctcct ggccttttct gcagggtgga cacagggtct 1620 gtgtgtgggc agcagcccct gtctctcagc aagaataaag cagcttcctg tgcaaaaaaa 1680 aaaaaa 1686 36 2350 DNA Homo sapiens misc_feature Incyte ID No 3434460CT1 36 cttgaaagga tcattgtgcg gattaaaaga aataatatat gtaaagcact ttaacacagc 60 accaggccca cggaaagtgg ctaatgttag ctactatgaa tggtgccagt gaagacactg 120 aaaaataagt gatttcagta accttctgga aagctatcag tttcaaataa tattttctct 180 gtaatatgag atgaaattaa aagtggatag ctttcaggaa agataaagag aacatgctta 240 gaatgtaagc taaacagatt ttttctgttg ctctttgaaa actatgagcc ctggccagct 300 taacctggtc tgaggtgaga ctaaacacaa aaacagtaga taaatctctc cctaaaagat 360 ggattccccc acatacccat gctactagtt tctctgtcta ttcacacata tgtacaaata 420 catgaacaca gcctgtctgt gctcagacat agagaagtac tacctgactt gagtcaatgc 480 acccaagaag aaaagcttgg agtagagcag aagggagggc ttgggactcc tgtctttcca 540 gcatgccctg gggtgcagtg gtcagccacc tgaagagaga gccaatagca tggggtttac 600 aaggcaaaga tagtcattca ttcaacacat attcatagag ctccttctct gtgccagaca 660 ctgttctgga agatagctag atgaaaatct ttgcactcac agagcttaca tgccagtgag 720 tgaagatcga tgataaataa agcaaatgca tcatatgttc acatttgata agtatatgcc 780 aaaaaatgaa gccgggaagg aggacaaggc ccatgggtgg gtgttgaggt ttttaaagtg 840 tggtcaggaa aggccccact gataaggtaa catttgagca agtctgaaaa aggcaagggg 900 atctttgggg ctaacttcgg gatccctgca ctttatgtaa gaatgtaaac ctggagtctc 960 atttaagaat gatcagcaat acgtttagaa catatgaact gaatgaaatg gacatttttt 1020 cttaatttac gtataaatcc atatgattat acataaagtt ctgatgcatt aataaaagca 1080 gccaaatagg gccaaagaga aaaataacag gactctgtac tggacctaac tttatcatta 1140 attaggtaat attttcctca tttctttact gctgccattt tcctcaccag tattccagag 1200 atggtcatag ctcattactc taccaccaag aacctaaaag gaattagaat acagcagaat 1260 tggcctcagt gaagagctta aaattgttct cctcgtagaa ctggactatt gatcattacc 1320 acgtgacgtt ggctctatta ctttctgttc ccaatgtcct tctagtggtt tgaaaatgtt 1380 aaaacatccc taaaatctaa atcatataat cagaattcta tagtgtccca ctctatctgt 1440 aaagatcatt tggaagactt tagactctat taattttaaa aggaatattt attagccata 1500 tgcagaattt ctaatgatga tattgtacag cttctaattc acttttcaga tcagtgtttg 1560 aaatggcaat tatcagtgtt ggatttagtt ccaactactt gatttacaaa aatgtacatt 1620 tagaggttaa aagaaacagt gagaaatgta aacattcaaa atgataattg aatctctcag 1680 ttgtgggaat aattatcaga gacatgcaac tgaaaatgtc tcacctttca tctttttttc 1740 ttaattcata aagttatctt gtagaatttg atgagaccct cctagtcatt ctcaactggg 1800 gcggtgctgt caccgaatgg tgtttgagag tgttggggct agggcacatt tttggttgtc 1860 acagcaactg gggtggcatt tgctgcccag tgccaggaat agtaacatta tgaatgccag 1920 ggacagtgtg ctcagtaaag tcttccatcc aaaaggggca gggcacggtg gctcacgcct 1980 gtaatcccag cactttggga ggccaaggtg ggcggatcac ctgatgtcag gggttcgaga 2040 ccagcctggc caacatggtg aaaccctgtt gctactaaaa atacaaaaat tggctgggtg 2100 tggtgtcaca tgccagtaac cccagctact agggaggctg aggcaggaga atcacttgaa 2160 cccgggaggc agaggttgca gtgagctgag attgcaccac tacactccag cctggatgac 2220 agagtgagac ttcatctcaa aaaaaaaaaa aaaagggcgg cagctctaga ggaaccaagc 2280 taacgtacgc gagcatgcga catcatagat cttctatagt gtcacctaat taatacatgg 2340 ccgtacagag 2350 37 3502 DNA Homo sapiens misc_feature Incyte ID No 5022769CT1 37 gcggccgctg acagcaccag catgtcttac agtgtgaccc tgactgggcc cgggccctgg 60 ggcttccgtc tgcagggggg caaggacttc aacatgcccc tcactatctc ccggatcaca 120 ccaggcagca aggcagccca gtcccagctc agccagggtg acctcgtggt ggccattgac 180 ggcgtcaaca cagacaccat gacccacctg gaagcccaga acaagatcaa gtctgccagc 240 tacaacttga gcctcaccct gcagaaatca aagcgtccca ttcccatctc cacgacagca 300 cctccagtcc agacccctct gccggtgatc cctcaccaga aggaccccgc tctggacacg 360 aacggcagcc tggtggcacc cagccccagc cctgaggcga gggccagccc aggcacccca 420 ggcaccccgg agctcaggcc cacctttagc cctgccttct cccggccctc cgccttctcc 480 tcactcgccg aggcctctga ccctggccct ccgcgggcca gcctgagggc caagaccagc 540 ccagaggggg cccgggacct actcggccca aaagccctgc cgggctcgag ccagccgagg 600 caatataaca accccattgg cctgtactcg gcagagaccc tgagggagat ggctcagatg 660 taccagatga gcctccgagg gaaggcctcg ggtgtcggac tcccaggagg gagcctccct 720 attaaggacc ttgccgtaga cagcgcctct cccgtctacc aggctgtgat taagagccag 780 aacaagccag aagatgaggc tgacgagtgg gcacgccgtt cctccaacct gcagtctcgc 840 tccttccgca tcctggccca gatgacgggg acagaattca tgcaagaccc tgatgaagaa 900 gctctgcgaa ggtcaagcac ccctattgag catgcgccgg tgtgcaccag ccaggccacc 960 accccgctgc tgcccgcttc tgcccagcca cctgctgctg cctctcccag tgcggcttcg 1020 ccacccctgg ccacagctgc tgcccacact gccatcgcct ccgcctccac cacagcccct 1080 gcttcaagtc ctgccgacag cccaaggccc caggcctctt cctacagccc cgcagtggcc 1140 gcctcttcag cacctgccac ccacaccagc tacagtgagg gccccgccgc ccctgcaccc 1200 aagccccggg ttgtcaccac tgccagcatc cggccttctg tctaccagcc agtgcctgca 1260 tctacctaca gcccgtcccc aggggccaat tacagtccca ctccctacac cccctcccct 1320 gcccctgcct acaccccctc ccctgcccct gcctacaccc cctcacctgt ccccacctac 1380 actccatccc cagcaccagc ctataccccc tcacctgccc ccaactataa ccctgcaccc 1440 tcggtggcct acagcggggg ccctgcggag cctgccagcc gtccaccctg ggtgacagat 1500 gatagcttct cccagaagtt tgccccgggc aagagcacca cctccatcag caagcagacc 1560 ctgccccggg gaggcccagc ctacacccca gcgggtcctc aggtgccacc acttgccagg 1620 gggaccgtcc agagggctga gcgattccca gccagcagcc ggactccact ctgcggtcac 1680 tgcaacaatg tcatccgggg cccatttctg gtagccatgg gccgttcttg gcaccctgaa 1740 gagttcacct gtgcctactg caagacttcc ctggcagatg tgtgctttgt ggaagagcag 1800 aacaacgttt actgtgagcg atgttatgag caattctttg ccccgctgtg tgccaagtgc 1860 aacaccaaaa ttatggggga agtaatgcat gccttgagac agacatggca caccacctgc 1920 ttcgtctgtg cggcctgcaa gaagcctttt gggaacagcc tcttccacat ggaagacggg 1980 gagccctact gcgagaaaga ctacatcaat ctgttcagca ccaagtgcca tggctgcgat 2040 ttccccgtgg aggctggcga caagtttatc gaagccctgg gccacacttg gcacgacacc 2100 tgcttcattt gcgcagtctg ccatgtgaat ctggaggggc agccgttcta ctccaagaag 2160 gacagacccc tgtgcaagaa gcacgcacac accatcaact tgtaggcggc caaggccgcc 2220 tgtgctgacg aggcccggag ctgctcctgc tgctggcaac aaaggattcg ggaggctgat 2280 gtttcttctg aggggaatgg ggagagagag gaagcgactg agccctttgg aagtataatt 2340 ttaggttttt tcttctgtac acagatcgtg catttgcata gttcagacta ggagccaaat 2400 gaagactcaa aaccaagcta gttattaatc caagactgga attgtacttc agacatttag 2460 agcagaattc caagaactca aaagtgaaaa gcaacaagca gctttcccaa agcgatacac 2520 ttgctttggt caccagagga ggacagagct tagagcagct gtggagaatc tgaagcattc 2580 tgcggagttc ttaagcgctc ccctggcaaa caaattgaag tgccaaacag cactcgctgc 2640 agggtatttt tagagtcata gctgagagct tgttagctaa gacccattgg gctttcctca 2700 ccaaaaaagg aagtgttatt ccattactag cgtcatggag ctacctctgc gcatcagact 2760 tcagaccttg aacaaactta aaaccttctt gggagcccgg acgtccaaag agatgtcttc 2820 tgggagccac tgggcaattg ccagggctcc aggaagggct ctggctcagg ttgcagacag 2880 ctgagaaaag atggccctgt cagccaccct ctctcagtct gaaacatcca acatccccag 2940 aaggcttagc tcctttttga attgtgatgg gaaagtagag ttgggttttt ccagttttgc 3000 tctgtggtgt gtgagagatt tttttaaagg ctttgggttg tctttggcct ttgtttagct 3060 ttaagggttc gttagcatga gtgtccagtc gtgtgcatga atttcacccc aacttgtgac 3120 tgctcactta tgacgtctcc cccagtaccc tccatctcaa ataggcttgg tggcctgtgg 3180 aaaagaagag agacagagag acagtgtctg aaacaggatg gcagaatagg ctcacatgcc 3240 caaactctgg gtggggaaga ggaaacttac tttctgccac cctcagtaag aacacacgag 3300 gaggcaggac ctcccacctt caggtctgca tcatcctttt caaatgttcc tttaaatgca 3360 gcacactgag tttgtacaat tgtgttaact gctggaaggg acagatgcac tgatatatat 3420 gcatttgctg ttttggccaa tattttgaaa atgtatgagc tgagttgatc tagctattat 3480 ttaagtattt attgaagtag ag 3502 38 1689 DNA Homo sapiens misc_feature Incyte ID No 944140CT1 38 cagacgtatg aagcatccat ggacaagctg agggaaaagc agaggcagtt ggaggtagcg 60 caagttgaaa accagctgct aaaaatgaag gtggaatcgt cccaagaagc caatgctgag 120 gtgatgcgag agatgaccaa gaagctgtac agccagtatg aggagaagct gcaggaagaa 180 cagaggaagc acagtgctga gaaggaggct cttttggaag aaaccaatag ttttctgaaa 240 gcgattgaag aagccaataa aaagatgcaa gcagcagaga tcagcctaga ggagaaagac 300 cagaggatcg gggagctgga caggctgatt gagcgcatgg aaaaggaacg tcatcaactg 360 caacttcaac tcctagaaca tgaaacagaa atgtctgggg agttaactga ttctgacaag 420 gaaaggtatc agcagttgga ggaggcatca gccagcctcc gtgagcggat cagacaccta 480 gatgacatgg tgcattgcca gcagaagaaa gtcaagcaga tggtcgagga gattgaatca 540 ttaaagaaaa agttgcaaca gaaacagctc ttaatactgc agcttttaga aaagatatct 600 ttcttagaag gagagaataa tgaactacaa agcaggttgg actatttaac agaaacccag 660 gccaagaccg aagtggaaac cagagagata ggagtgggct gtgatcttct acccagccaa 720 acaggcagga ctcgtgaaat tgtgatgcct tctaggaact acaccccata cacaagagtc 780 ctggagttaa ccatgaagaa aactctgact taggcactca gaggcataca ctttttacag 840 atggacaaaa gctctggaac cctgtggctt caaatccttt gggaagggtg actgttgttt 900 cccctacaca cagtgtaagc cggaatggga atcgctgagg ctctgatcca cttctaagac 960 aggaaggaaa gtgaaggcag agtgagcagg taagagaggg atatacaagg tcacatttca 1020 gacacccact cggcataccc tgccgtactg catcatcatt tgttttcttt gtagacactg 1080 aaatcctatc aggaggattc cttcacaatg tattttattt gctagacttt ggttgggagg 1140 gaaaaggaca ttaatttgaa gtttcatgtt attcatgcca ggattgtttg atagagcatg 1200 aaggttttgt ttacccataa aagtattaga ggcagcgttt ctctgataca gagaggcctg 1260 tccacaagaa gcatgggcac ccagccaaac ttgaacctgg aagggagggt tcccggcctg 1320 caggtgctct ttcctcttgg tcccaagcat ctgtgcaggg tcgtgggagc cacactgaga 1380 gacttgtgtg ggccagacaa gcttcattct gatgcgctag tcccttggtt taatttgtgc 1440 cttatgcttt cattggacca gctgaaatca ctgtatttat tcaacttgtg attttttttt 1500 ctttctcact ttaacttaaa gagaatttta tatgtcttgg aaatttaata atttagtgtt 1560 ctcagtatca attggtgttt ttgttaaacg aatgaatcat ctgttcatgc atgctctact 1620 ttgatattat aacctatgtc acatgtgttt aataaatacc atatattttg ttctaaaaaa 1680 aaaaaaaaa 1689 39 1918 DNA Homo sapiens misc_feature Incyte ID No 3445829CB12 39 cagcctgcca cttgcctccc tgcctgcttc tggctgcctt gaatgcctgg tccttcaagc 60 tccttctggg tctgacaaag cagggaccat gtctaccttt ggctaccgaa gaggactcag 120 taaatacgaa tccatcgacg aggatgaact cctcgcctcc ctgtcagccg aggagctgaa 180 ggagctagag agagagttgg aagacattga acctgaccgc aaccttcccg tggggctaag 240 gcaaaagagc ctgacagaga aaacccccac agggacattc agcagagagg cactgatggc 300 ctattgggaa aaggagtccc aaaaactctt ggagaaggag aggctggggg aatgtggaaa 360 ggttgcagaa gacaaagagg aaagtgagga agagcttatc tttactgaaa gtaacagtga 420 ggtttctgag gaagtgtata cagaggagga ggaggaggag tcccaggagg aagaggagga 480 agaagacagt gacgaagagg aaagaacaat tgaaactgca aaagggatta atggaactgt 540 aaattatgat agtgtcaatt ctgacaactc taagccaaag atatttaaaa gtcaaataga 600 gaacataaat ttgaccaatg gcagcaatgg gaggaacaca gagtccccag ctgccattca 660 cccttgtgga aatcctacag tgattgagga cgctttggac aagattaaaa gcaatgaccc 720 tgacaccaca gaagtcaatt tgaacaacat tgagaacatc acaacacaga cccttacccg 780 ctttgctgaa gccctcaagg acaacactgt ggtgaagacg ttcagtctgg ccaacacgca 840 tgccgacgac agtgcagcca tggccattgc agagatgctc aaagtcaatg agcacatcac 900 caacgtaaac gtcgagtcca acttcataac gggaaagggg atcctggcca tcatgagagc 960 tctccagcac aacacggtgc tcacggagct gcgtttccat aaccagaggc acatcatggg 1020 cagccaggtg gaaatggaga ttgtcaagct gctgaaggag aacacgacgc tgctgaggct 1080 gggataccat tttgaactcc caggaccaag aatgagcatg acgagcattt tgacaagaaa 1140 tatggataaa cagaggcaaa aacgtttgca ggagcaaaaa cagcaggagg gatacgatgg 1200 aggacccaat cttaggacca aagtctggca aagaggaaca cctagctctt caccttatgt 1260 atctcccagg cactcaccct ggtcatcccc aaaactcccc aaaaaagtcc agactgtgag 1320 gagccgtcct ctgtctcctg tggccacacc tcctcctcct ccccctcctc ctcctcctcc 1380 ccctccttct tcccaaaggc tgccaccacc tcctcctcct ccccctcctc cactcccaga 1440 gaaaaagctc attaccagaa acattgcaga agtcatcaaa caacaggaga gtgcccaacg 1500 ggcattacaa aatggacaaa aaaagaaaaa agggaaaaag gtcaagaaac agccaaacag 1560 tattctaaag gaaataaaaa attctctgag gtcagtgcaa gagaagaaaa tggaagacag 1620 ttcccgacct tctaccccac agagatcagc tcatgagaat ctcatggaag caattcgggg 1680 aagcagcata aaacagctaa agcgggtaag taaccagaga acagacatag gggcacagat 1740 aaagtaaatg agttgtcctc cattgcatgg tggtaccaaa gtcacctctc acaatactta 1800 tcaatacttt caatatttta gtatgcgaga gcaaacacac caagtttgaa acattaggag 1860 caggcacaca agtgagcaca tttctatttg agaggaacgc ctgggccgct ttcccagg 1918 40 1086 DNA Homo sapiens misc_feature Incyte ID No 3016490CT1 40 gcggccgcta cggcgtcttc gtcaagatca agtatggctc cgagacgggc cagggcacca 60 ttagtgtgtt caagcacggg gacgagccca aggagctgaa gagcatgtga cagcgtgtgt 120 ccaggcacag tctgagtcta gtctgcatgg accagtaggg acaacctgta ccagggtcac 180 agcctggcac aggctacagg ggtggggcag aaggaaaggg gacaagatag aacccaggat 240 gtgagggtgg gggtggagcg gatgcaccaa agtggagaag caaagatctt tctggggtcc 300 tgagtggctt ccaggagagc gggatgaacc ctggacctgg agtaggagac ccggatgcac 360 tggggctatc taacagtact ggcatctgat aggtagaggt caggtacgct gctaaacact 420 gcagctccca ccacatagaa ttatccgacc ccagatgtca aaagtgccaa gggccatgag 480 ccctgccata aactgataca tcgcacccct cttttaggat cccatagttt caattcatgt 540 aagttcaaca gacacctgaa gtctagcatg tgggaggctg aggatggagc tgggaacaca 600 aaggcagctg ataagcaggt tctgcttgca aagaggcctc agtccagtgg gagaaacaga 660 cctgggcgca aacaactcca ggacaaggca ggacatgata aagattataa agcaggtcca 720 aggaaagtgc cgccagtggt ccaaggaggg agacagaggg tcgtcccaac agggggaggt 780 agggctttga aaacaccttc atccaggctg ggcgaggtgg ctcacgcctg taatcccagt 840 agtttgggag gccaaggcgg gcagatcacc tgaggtcagg agttttagac cagcctggcc 900 aacatgacga aactcagtct ctactaaaaa tacaaaaatt agccaggcat ggtgggcagt 960 agctgtaatc ccggctattc agaaggccga ggtgggagaa tccgttgaaa cttgggaggc 1020 ggaggttgtg aattgagcca gatttgggcc aaaaaaaaaa ttggccgaaa ttggtgtttg 1080 ggcccc 1086 41 3441 DNA Homo sapiens misc_feature Incyte ID No 4151935CB1 41 gtttcaaagg acacaaagag agatgtggac tcaaagtcac cggggatgcc tttatttgaa 60 gcagaggaag gagttctatc acgaacccag atatttccta ccactattaa agtcattgat 120 ccagaatttc tggaggagcc acctgcactt gcatttttat ataaggatct gtatgaagaa 180 gcagttggag agaaaaagaa ggaagaggag acagcttctg aaggtgacag tgtgaattct 240 gaggcatcat ttcccagcag aaattctgac actgatgatg gaacaggaat atattttgag 300 aagtacatac tcaaagatga cattctccat gacacatctc taactcaaaa ggaccagggc 360 caaggtctgg aagaaaaacg agttggtaag gatgattcat accaaccgat agctgcagaa 420 ggggaaattt ggggaaagtt tggaactatt tgcagggaga agagtctgga agaacagaaa 480 ggtgtttatg gggaaggaga atcagtagac catgtggaga ccgttggtaa cgtagcgatg 540 cagaagaaag ctcccatcac agaggacgtc agagtggcta cccagaaaat aagttatgcg 600 gttccatttg aagacaccca tcatgttctg gagcgtgcag atgaagcagg cagtcacggt 660 aatgaagtcg gaaatgcaag tccagaggtc aatctgaatg tcccagtaca agtgtccttc 720 ccggaggaag aatttgcatc tggtgcaact catgttcaag aaacatcact agaagaacct 780 aaaatcctgg tcccacctga gccaagtgaa gagaggctcc gtaatagccc tgttcaggat 840 gagtatgaat ttacagaatc cctgcataat gaagtggttc ctcaagacat attatcagaa 900 gaactgtctt cagaatccac acctgaagat gtcttatctc aaggaaagga atcctttgag 960 cacatcagtg aaaatgaatt tgcgagtgag gcagaacaaa gtacacctgc tgaacaaaaa 1020 gagttgggca gcgagaggaa agaagaagac caattatcat ctgaggtagt aactgaaaag 1080 gcacaaaaag agctgaaaaa gtcccagatt gacacatact gttacacctg caaatgtcca 1140 atttctgcca ctgacaaggt gtttggcacc cacaaagacc atgaagtttc aacgcttgac 1200 acagctataa gtgctgtaaa ggttcaatta gcagaatttc tagaaaattt acaagaaaag 1260 tccttgagga ttgaagcctt tgttagtgag atagaatcct tttttaatac cattgaggaa 1320 aactgtagta aaaatgagaa aaggctagaa gaacagaatg aggaaatgat gaagaaggtt 1380 ttagcacagt atgatgagaa agcccagagc tttgaggaag tgaagaagaa gaagatggag 1440 ttcctgcatg agcagatggt ccactttctg cagagcatgg acactgccaa agacaccctg 1500 gagaccatcg tgagagaagc agaggagctt gatgaggccg tcttcctgac ttcgtttgag 1560 gaaatcaatg aaaggttgct ttctgcaatg gagagcactg cttctttaga gaaaatgcct 1620 gctgcgtttt ccctttttga acattatgat gacagctcgg caagaagtga ccagatgtta 1680 aaacaagtgg ctgttccaca gcctcctaga ttagaacctc aggaaccaaa ttctgccacc 1740 agcacaacaa ttgcagttta ctggagcatg aacaaggaag atgtcattga ttcatttcag 1800 gtttactgca tggaggagcc acaagatgat caagaagtaa atgagttggt agaagaatac 1860 agactgacag tgaaagaaag ctactgcatt tttgaagatc tggaacctga ccgatgctat 1920 caagtgtggg tgatggctgt gaacttcact ggatgtagcc tgcccagtga aagggccatc 1980 tttaggacag caccctccac ccctgtgatc cgcgctgagg actgtactgt gtgttggaac 2040 acagccacta tccgatggcg gcccaccacc ccagaggcca cggagaccta cactctggag 2100 tactgcagac agcactctcc tgagggagag ggcctcagat ctttctctgg aatcaaagga 2160 ctccagctga aagttaacct ccaacccaat gataactact ttttctatgt gagggccatc 2220 aatgcatttg ggacaagtga acagagtgaa gctgctctca tctccaccag aggaaccaga 2280 tttctcttgt tgagagaaac agctcatcct gctctacaca tttcctcaag tgggacagtg 2340 atcagctttg gtgagaggag acggctgacg gaaatcccgt cagtgctggg tgaggagctg 2400 ccttcctgtg gccagcatta ctgggaaacc acagtcacag actgcccagc atatcgactc 2460 ggcatctgct ccagctcggc tgtgcaggca ggtgccctag gacaagggga gacctcatgg 2520 tacatgcact gctctgagcc acagagatac acatttttct acagtggtat tgtgagtgat 2580 gttcatgtga ctgagcgtcc agccagagtg ggcatcctgc tggactacaa caaccagaga 2640 cttatcttca tcaacgcaga gagcgagcag ttgctcttca tcatcaggca caggtttaat 2700 gagggtgtcc accctgcctt tgccctggag aaacctggaa aatgtacttt gcacctgggg 2760 atagagcccc cggattctgt aaggcacaag tgatccttgg ctttcagaat ttgcaagaac 2820 agcgatttga attttggggg ggtctgctgt tcattccttt aggtgctata cattattcaa 2880 aaagtctccc gcgcatttgc actaatgatg gctgcatgca tagcaatcag catgtgagca 2940 aaatcgacaa gaaaaccttg actttacaga gcagtgtgtg agtaaacaga atgaaaacaa 3000 caacctccac tctttagttt atataagttt gagttctttc ctaaattaaa agatctacac 3060 ttgagttggg aaccaaaaga gaaaaatgga cttccatctg ttttactggt aaaggaaatc 3120 ctctgatgga caggtcagag tgaaggaagg ttgtgctggt aagacatctc tgacgaagag 3180 ccatggatgc tttccacaaa atgtcacctc gctgcactaa aggatgatga atcctaatca 3240 ttaaaggaat tgtttcagct gatttaaatt tataatgaac tcttttgtaa taatgtatac 3300 tgtagaacat gagtctctcc tccctaaaat tttaaatgta gaaaagtgct atatattaga 3360 aatttccatt ttgttaaata aatggttaga gtctataaag ccagtcatgt tatgtgaact 3420 tactccatgt aacttactgg c 3441 42 1461 DNA Homo sapiens misc_feature Incyte ID No 3719652CT1 42 cactaagaag gggctgtgct ttgatcccct gcctcttgca ctaccaatgt ctcaagacat 60 aatattcatc tcttgctgtc agacccattc tatattctaa aagcttctgc tccttccttc 120 ccaatttctc ctttgtagca ggaaattaca cccagccctc atctcaatta atgctaaata 180 aagctattgt ttttccaaaa cacaaatcta cactgggtct caatatcagt gatgaggctt 240 acaaaccaac acgttttctg ccatgaggat ttctctttag gccagaagta caaaacaaaa 300 aaaccaatgg attttaacca aaatgatttg aaatataggt gaggattcag gagaaggcaa 360 aagctagaaa cacttggggt tgtcaacatg agtattacat taacattgct tgatgagaac 420 ctctaatgat actgacaaca taaattacct agggtaaagg atagctgcaa caatgaaaca 480 ggaaagaaga gagggagaga gaggaaaggg aaggaagaaa ggaaggaggg agaagggaag 540 aaagaaacaa tgtctaaccc aaccctatct tgaaagttga actcaagtag aaaaatggat 600 agaaacaaaa ttctctagta ctcatccagg aaaccattct tcaatgttgc atgtggctgt 660 ttgccaaggc acacaaagtg cttgtaggca gcaaccatat gctacaagaa ttgtaaactg 720 catacagttt gtttgaagta gacagtgagg ataataacaa agttgctagg caggaaaaaa 780 aatcaggaaa aaagcttgtc gctatttgag aatctgtata tttttaaagg cttaaaatat 840 tataaccaca gggtatccag ccaaattcaa cattactgca agtcttagag atttaaacat 900 tcatttgatt catagctaaa tattcaccat aatccaggag ggtctccttc cccactgcag 960 aggcagaacg tccaagaatg gagtaagatt agtcatagta aagtctcagt ctgaatattt 1020 agcaagagaa acaggcagca gaggaaccca aaggcagtaa atcaaatatt ctaaaaccca 1080 aagttcatta ttttcatcca aaagactttc acagaaacac attactcaca gccatgtata 1140 tcttggacag agtttcagat ggaatgactt gtctgaaatt tgtaaagctt aatataggtt 1200 ttgggggaat tattttaata ttcaaagaat gttttattat agtcctttgt gttaaaattt 1260 agccttacta attataacaa taactcataa agttctaaat tcagaaggaa tgtctgttct 1320 ttatcaagtg tatgtaacta ttttttagaa atgccatcta ctttctagaa acactaaagt 1380 tattgttttc taagttaaat aactataatt tatatatcta ttaaaaaggt acttctcttc 1440 ccaaaaaaaa aaaaaaaaaa a 1461 43 854 DNA Homo sapiens misc_feature Incyte ID No 3046106CT1 43 ttttgaagta tttttaaaag gggtttggag gtagcatccg aaatcatata aagattgggg 60 ataaatgttg aatttttgag atatggaatg tctattaaga ggtggaataa agattgtatg 120 tgtcatactc tttggaggaa agtggtcccc caaaatgaca gcaattccta aggagtttgt 180 gaaggggtac atgttggaat catatagagt aaatatcata aaaactatcc atacattact 240 gttgcattgg caagagcaca tcatttagaa tatacatcca attattaaat ttatttaata 300 ggcaagatgt tatagagaag acagttctca agattctttt tcagtttcca ttgactaaat 360 ttctaacttt agaaagctct gaatgtgaca tatttcgcca ttcttcagca agagtgatgt 420 caaacttaca tccccacttt gcaaaaatat atcacttcaa tggaggtggc atataaacct 480 gaatttttat tttatggaag gttgctatgt gaatatacag agctgaaggt ttaggagggc 540 aactaagggt cttatcgtac cacatctctg gcccttattg aatgtttctt ttcctaagtc 600 cattcctgac tccagtttgc tgtataatcc tgagactcct ttacagaata cggggatcta 660 acatgtagag actattcctg taattggtgt ttcttggagg cattgcaaaa ccaaattttt 720 ctttactttg tagcactttt gactaatgtt atctaaggac tgtatcaaag aattggtttc 780 tattagattt tagtttaaga aatcttacaa ttttgttaca gagcaggcta tttggaggat 840 gaaactgaaa ttaa 854 44 714 DNA Homo sapiens misc_feature Incyte ID No 3012947CB1 44 accctttcag taatcattca accaacgctt ccatgtctct actctgtcgt aacaaaggct 60 gtgggcagca ctttgaccct aataccaacc ttcctggtca gagttgcctc tgaagctgct 120 gccgctaaat atatcccaag ccctggaaat ggcattggaa cagaaggaat tagaccagga 180 acctggggca ggacttgaca gtctgatccg gactggttcc agctgccaga acccaggatg 240 tgatgctgtt taccaaggcc ctgagagtga tgctactcca tgtacctacc acccaggagc 300 accccgattc catgagggga tgaagtcttg gagctgttgt ggcatccaga ccctggattt 360 tggggcattc ttggcacaac cagggtgcag agtcggtaga catgactggg ggaagcagct 420 cccagcatct tgccgccatg attggcacca gacagattcc ttagtagtgg tgactgtata 480 tggccagatt ccacttcctg cgtttaactg ggtgaaggcc agtcaaactg agcttcatgt 540 ccacattgtc tttgatggta accgtgtgtt ccaagcacag atgaagctct ggggggtaag 600 tgaagaccag gggacacaag agtgggaggc agatgggtga aagagcggct agactggaat 660 agagggtgtc ttgagggaag gagttgtact aggaaaatgg aggttttctc ttca 714 45 1434 DNA Homo sapiens misc_feature Incyte ID No 466761CT1 45 caagaatgta tcctttcagc tctctttggt tatacctgaa gccaggagcg ttgagttatt 60 agccttgtgt ttatattcct ctcactgtaa ttggtgtcat tttcccagca gtcctagcag 120 tcctcaagca agtgggaaat cggaaaagaa aaggacaggc attgtaggga agcagaggat 180 aaagaattta gccaacaaaa gaaacaatct agtcaatctg ggtgctttta tttcctgggt 240 actctctaaa catggctcag agctggtgta gatgaagtag gtgaaacctc tgaaaagagt 300 ctagaaggca gtagagcaag tcccagacca gaaacatgct catcttttca tcgtaatgtg 360 ccactcggta ctatttggta atgtcactct atttttccta atcccatcct ttggtttgta 420 tttcatattt gtatataagg caccattttc taaaaatatg actagggtgt gacctaaggt 480 tttattctgt gaagatgagt aactggaaag aagctaacac tgcagtggga aggaaggaag 540 agagttgtcc aggtggtagt tcgacgtgtt ttgaatctag tccttcctac atggaggata 600 aaagctccta aagtccactc tgggtttgtg attttaatag aaatagaaag ggaaactata 660 gaccaatgga gatgaaaatc aggggctatc gacagatgga ggagaaataa ggtgctacat 720 agagaaagga agagggcaga aggctttccc ttcccaaact gggtgagctg gggaagcctt 780 ggttcaggag agtggcactg cccacaactg ctttgtgggt tgtgcacttc cagccgcact 840 ctccccctcc agttgctgcc ttcagagccg tactgaagca cgagcttcaa taagacaagc 900 acacttcata gtgagagggc agcggtacca aagcctttca gagagactat ggattagaca 960 gaaatgattt gtgagaggaa gctggagtga acagcatgaa cagcgagtgt tacctgacag 1020 aggcaagaca gctagaagtg gcttcagatt tagaaacagc tgaggggagc aaagacggac 1080 tgtgtacaca gggagggagg atgtctatgg gcagagccct tggtgagtat catcaccaag 1140 aaaggcagtc cagagtagag atcagccgaa tatggaggct gaggtctgta gaactgggcc 1200 agagaggacc ttactgcctt agtagcataa gggtctggaa aagaagtttc tatctcacaa 1260 caaaggaaaa agtgaaaagc aaggtggaac ttgaagatac gtcacgaaaa tcactataaa 1320 agtctgattt atgtgtgatg tcaaatcaaa ctgaaatgaa gaatgagatt gagtatatct 1380 gtggtgactg acctctgtat actagaaacc tcaacatctc tagaagagga aata 1434 46 2298 DNA Homo sapiens misc_feature Incyte ID No 1644171CT1 46 tgagaaccaa ctcattttgg tatttttagt agagacgaaa ccccatcctc ccaaagtgct 60 gggattacag gcatgagctg ccgcacccgg cctccacctg ggttttgagc caatcccctg 120 gacttgctcc tggtttcctc aaggggtggg gcagtggttt aggacactcg acaactaaga 180 acaggagttc ccaggaagga caaggatctg catcccccac tgccacttct ctgatgtgtt 240 cctcaaagct ggctcgaggg ctcgatccct tcatcggact caggagggga ctggttggtg 300 tatccaggta atttactctt ggaagtgact gtagtgaagg tcgtggaagg gctcagaggg 360 ttaattggtt tgcagtgcgt ctttgtctat tgcatgtctt ggaaaactca gatcccaaag 420 gcgctgggtt tcagagagga cagtggagac cttgctcctt ttccttaggc cgccagtctc 480 tcaaatttca gaggaggctg tttccacaac tcccctatgg aaacacttgg cagcggagtt 540 gctcctttgc agtttccaca ccatggcttt tcctttcctt tcttctccat tccctgatgc 600 atcaacactt acttggagca atttcctagg agtcagaacc agcaccagcc actcggtgtc 660 ggtggccacc aaggcttaac attgaccttc ccgcctgacc ttgatgcaga tgtccactga 720 acacaccgca ggaaagccag ggccttcaat accaataagt gtgaatatgt gtgtatgttg 780 tccaagagag attagggaga tcacatagac tctagggagt agagaacttg taacagtctt 840 gcaaggctag catgcacggc tccacagcag gtggtgggga gcagaggggc aggacctgca 900 gggaagaagc agcctttgga tggtgaaatg tgcatggtgc acagtctgtg catgcccagg 960 agacccagcc cgggctgcct cgaggggctc ctttgtacac agccagccgc ttctcttggg 1020 aacaagctgt cctgggggcc ttacccacga ggcaggagtc aggatgcacc agctcagcac 1080 caggaagtca tcctggaccc aggacagtgg aaaggcaggc agagggagag gcactctgag 1140 gtcaggcagg gtaagccagt tggcagtcag gttaggtcta tgaggagaac ctcgagttag 1200 gaattcccgg ttctcagaat tgttatcact ctggtgcatg ctgtcacagg ggccgttgcg 1260 tttggctttg tggagggcct ggacccttcc acaagaacac ccgaggttcc agggcactca 1320 ggacaatgtt tccaaggaac gagtcgacca ggaaagaaca gtgagttctg caaggggcat 1380 ccacggagcc tgtgataggg gctgatgaga tggaatctgt cctggacttt tcttctcatt 1440 aaccaccctc cgcaaacccc agaacccctc gcctcatctc tgtactgtct gccctcttgg 1500 gggatgggcc ctcccacttt cccctgcctg ctcctccatg ctgtgagctg ctttggcaga 1560 tctgtttttc tgtgtagtca ggggaaaaac aaaaaaagat gcacaactgt gtgggcattg 1620 tcatagctgt tggtgtcacc actgctttgg gggaaatggc tgggatgagg ctaatacatt 1680 catgcaatat ttatattttc agggggctgc gttatcagca tgctctccct gccttgggct 1740 tttctttccg tcatgttttc cttttcgtgt tccttctctg atttctcttg tctctgctgc 1800 tcacaggcct gcccatcagt cagtacagat actcagtgtc tggtttctgg ccagctccgt 1860 ggagggggct ttaagcagaa ttctgactct ttggggtggg ggattaggaa ctgggggaaa 1920 cttaatgatc cagagattcc cccaagagga gtgtctggaa ggatctgtgc ctggacagtg 1980 gcagaacctt tccagtgttc ttttggttct gatttcatca gtctcaataa agttccgatc 2040 tctctttaaa aaaaaaaaaa aacaaaaaaa aaaaaaaaaa aaaaaaaaaa agacaaaaaa 2100 aaaaaagggg gccccccaaa agggggggga ccccgcccca agcgcgaaag cgcctcaana 2160 gctttcccnn gaaaaaattt ttcccccccc aaaattccag cccgctggtg gagtcgcctg 2220 tcnnnnnnnn nnnnnnnnnn nnnnnctnnn nnnnnnnnnn nnnnnnnnnn nnggnnncnn 2280 nnnnnnnnnn nnnnnccc 2298 47 728 DNA Homo sapiens misc_feature Incyte ID No 3009806CB1 47 gacaataggg agaatggaga acgtggaggt cttcaccgct gagggcaaag gaaggggtct 60 gaaggccacc aaggagttct gggctgcaga tatcatcttt gctgagcggg cttattccgc 120 agtggttttt gacagccttg ttaattttgt gtgccacacc tgcttcaaga ggcaggagaa 180 gctccatcgc tgtgggcagt gcaagtttgc ccattactgc gaccgcacct gccagaagga 240 tgcttggctg aaccacaaga atgaatgttc ggccatcaag agatatggga aggtgcccaa 300 tgagaacatc aggctggcgg cgcgcatcat gtggagggtg gagagagaag gcaccgggct 360 cacggagggc tgcctggtgt ccgtggacga cttgcagaac cacgtggagc actttgggga 420 ggaggagcag aaggacctgc gggtggacgt ggacacattc ttgcagtact ggccggcgca 480 gagccagcag ttcagcatgc agtacatctc gcacatcttc ggagtgatta actgcaacgg 540 ttttactctc agtgatcaga gaggcctgca cagcgtgggg cgtaaggatc tttccccacc 600 tggggctggt gaaccatgac tgttggccca actgtaactg gcaaatttta caatgggcat 660 cctgagggca ttgaaatccc aaggttcatt accaagattg ggaatttgag cctccgggcc 720 ccttaggg 728 48 1158 DNA Homo sapiens misc_feature Incyte ID No 5578191CB1 48 cagctcgagg gacggcacca tggaggactc cgaggcggtg cagagggcca cagcgctcat 60 cgagcagcgg ctggcacagg aggaggagaa tgagaaactc cgaggagaca cacgccagaa 120 gctgcccatg gacttgctgg tgctggagga tgagaagcac cacggggctc agagtgcagc 180 cctgcagaag gtgaagggcc aagagcgcgt gcgcaagacg tccctggacc tgcggcggga 240 gatcatcgat gtgggcggga tccagaacct catcgagctg cggaagaaac gcaagcagaa 300 gaagcgggac gctctggccg cctcgcatga gccgccccca gagcccgagg agatcactgg 360 ccctgtggat gaggagacct tcctgaaagc tgcggtggag gggaaaatga aggtcattga 420 gaagttcctg gctgacgggg ggtcagccga cacgtgcgac cagttccgtc ggacagcact 480 gcaccgagct tccctggaag gccacatgga aatcctggag aagcttctag ataatggggc 540 cactgtggac ttccaggatc ggctggactg cacagccatg cattgggcct gccgcggggg 600 ccacttagag gtggtgaaac ttctgcaaag ccatggagca gacaccaatg tgagggataa 660 gctgctgagc accccgctgc acgtggcagt ccggacaggg caggtggaga ttgtggagca 720 ctttctatcc ctgggcctgg aaatcaatgc cagagacagg gaaggggata ctgccctgca 780 tgacgctgtg aggctcaacc gctacaaaat catcaaactg ctgctcctgc atggggctga 840 catgatgacc aagaacctgg caggaaagac cccgacggac ctggtgcagc tctggcaggc 900 tgatacccgg cacgccctgg agcatcctga gccgggggct gagcataacg ggctggaggg 960 gcctaatgat agtgggcgag agacccctca gcctgtgcca gcccagtgaa tgcgtgcccc 1020 agcccagcca gctacccagc ccctctctgt gtgcagccgg agggtcctaa gaatggctcc 1080 cggagctaac tgagggccca gccttttttc tgcatgatcc aggagcacat accacaaact 1140 accacaataa aaaagctg 1158 49 70 PRT Homo sapiens misc_feature Incyte ID No 3601719CD1 49 Met Leu Glu Pro Ser Arg Gln Ile Ser Ile Phe Gln Trp Glu Pro 1 5 10 15 Phe Gly Gln Glu Gln Val Asn Pro Pro Glu Glu Lys Asn Val Leu 20 25 30 Leu Lys Trp Arg Arg Val Phe Leu Pro Pro Arg Met Arg Arg Arg 35 40 45 Ser Gln Phe Gln Glu Arg Arg Asn Phe Gln Asp Leu Gln Ser Ile 50 55 60 Tyr Arg Lys Ser Arg Ile Leu Lys Val Asn 65 70 50 552 PRT Homo sapiens misc_feature Incyte ID No 3445829CD1 50 Met Ser Thr Phe Gly Tyr Arg Arg Gly Leu Ser Lys Tyr Glu Ser 1 5 10 15 Ile Asp Glu Asp Glu Leu Leu Ala Ser Leu Ser Ala Glu Glu Leu 20 25 30 Lys Glu Leu Glu Arg Glu Leu Glu Asp Ile Glu Pro Asp Arg Asn 35 40 45 Leu Pro Val Gly Leu Arg Gln Lys Ser Leu Thr Glu Lys Thr Pro 50 55 60 Thr Gly Thr Phe Ser Arg Glu Ala Leu Met Ala Tyr Trp Glu Lys 65 70 75 Glu Ser Gln Lys Leu Leu Glu Lys Glu Arg Leu Gly Glu Cys Gly 80 85 90 Lys Val Ala Glu Asp Lys Glu Glu Ser Glu Glu Glu Leu Ile Phe 95 100 105 Thr Glu Ser Asn Ser Glu Val Ser Glu Glu Val Tyr Thr Glu Glu 110 115 120 Glu Glu Glu Glu Ser Gln Glu Glu Glu Glu Glu Glu Asp Ser Asp 125 130 135 Glu Glu Glu Arg Thr Ile Glu Thr Ala Lys Gly Ile Asn Gly Thr 140 145 150 Val Asn Tyr Asp Ser Val Asn Ser Asp Asn Ser Lys Pro Lys Ile 155 160 165 Phe Lys Ser Gln Ile Glu Asn Ile Asn Leu Thr Asn Gly Ser Asn 170 175 180 Gly Arg Asn Thr Glu Ser Pro Ala Ala Ile His Pro Cys Gly Asn 185 190 195 Pro Thr Val Ile Glu Asp Ala Leu Asp Lys Ile Lys Ser Asn Asp 200 205 210 Pro Asp Thr Thr Glu Val Asn Leu Asn Asn Ile Glu Asn Ile Thr 215 220 225 Thr Gln Thr Leu Thr Arg Phe Ala Glu Ala Leu Lys Asp Asn Thr 230 235 240 Val Val Lys Thr Phe Ser Leu Ala Asn Thr His Ala Asp Asp Ser 245 250 255 Ala Ala Met Ala Ile Ala Glu Met Leu Lys Val Asn Glu His Ile 260 265 270 Thr Asn Val Asn Val Glu Ser Asn Phe Ile Thr Gly Lys Gly Ile 275 280 285 Leu Ala Ile Met Arg Ala Leu Gln His Asn Thr Val Leu Thr Glu 290 295 300 Leu Arg Phe His Asn Gln Arg His Ile Met Gly Ser Gln Val Glu 305 310 315 Met Glu Ile Val Lys Leu Leu Lys Glu Asn Thr Thr Leu Leu Arg 320 325 330 Leu Gly Tyr His Phe Glu Leu Pro Gly Pro Arg Met Ser Met Thr 335 340 345 Ser Ile Leu Thr Arg Asn Met Asp Lys Gln Arg Gln Lys Arg Leu 350 355 360 Gln Glu Gln Lys Gln Gln Glu Gly Tyr Asp Gly Gly Pro Asn Leu 365 370 375 Arg Thr Lys Val Trp Gln Arg Gly Thr Pro Ser Ser Ser Pro Tyr 380 385 390 Val Ser Pro Arg His Ser Pro Trp Ser Ser Pro Lys Leu Pro Lys 395 400 405 Lys Val Gln Thr Val Arg Ser Arg Pro Leu Ser Pro Val Ala Thr 410 415 420 Pro Pro Pro Pro Pro Pro Pro Pro Pro Pro Pro Pro Pro Ser Ser 425 430 435 Gln Arg Leu Pro Pro Pro Pro Pro Pro Pro Pro Pro Pro Leu Pro 440 445 450 Glu Lys Lys Leu Ile Thr Arg Asn Ile Ala Glu Val Ile Lys Gln 455 460 465 Gln Glu Ser Ala Gln Arg Ala Leu Gln Asn Gly Gln Lys Lys Lys 470 475 480 Lys Gly Lys Lys Val Lys Lys Gln Pro Asn Ser Ile Leu Lys Glu 485 490 495 Ile Lys Asn Ser Leu Arg Ser Val Gln Glu Lys Lys Met Glu Asp 500 505 510 Ser Ser Arg Pro Ser Thr Pro Gln Arg Ser Ala His Glu Asn Leu 515 520 525 Met Glu Ala Ile Arg Gly Ser Ser Ile Lys Gln Leu Lys Arg Val 530 535 540 Ser Asn Gln Arg Thr Asp Ile Gly Ala Gln Ile Lys 545 550 51 260 PRT Homo sapiens misc_feature Incyte ID No 2837330CD1 51 Met Ser Leu Leu Trp Thr Pro Lys Gly Lys Met Arg Leu Gln Ala 1 5 10 15 Glu Lys Leu Asn Lys Ala Pro Gln Gly Gly Ile Gly Thr Ala Ala 20 25 30 Val Arg Pro Lys Ser Leu Ala Ile Ser Ser Ser Leu Val Ser Asp 35 40 45 Val Val Arg Pro Lys Thr Gln Gly Thr Asp Leu Lys Thr Ser Ser 50 55 60 His Pro Glu Met Leu His Gly Met Ala Pro Gln Gln Lys His Gly 65 70 75 Gln Gln Tyr Lys Thr Lys Ser Ser Tyr Lys Ala Phe Ala Ala Phe 80 85 90 Pro Thr Asn Thr Leu Leu Leu Glu Gln Lys Thr Pro Thr Thr Leu 95 100 105 Pro Arg Ala Ala Gly Arg Glu Thr Lys Tyr Ala Asn Leu Ser Ser 110 115 120 Pro Thr Ser Thr Val Ser Glu Ser Gln Leu Thr Lys Pro Gly Val 125 130 135 Ile Arg Pro Val Pro Val Lys Ser Arg Ile Leu Leu Lys Lys Glu 140 145 150 Glu Glu Val Tyr Glu Pro Asn Pro Phe Ser Lys Tyr Leu Glu Asp 155 160 165 Asn Ser Asp Leu Phe Ser Glu Gln Asp Val Thr Val Pro Pro Lys 170 175 180 Pro Val Ser Leu His Pro Leu Tyr Gln Thr Lys Leu Tyr Pro Pro 185 190 195 Ala Lys Ser Leu Leu His Pro Gln Thr Leu Ser His Ala Asp Cys 200 205 210 Leu Ala Pro Gly Pro Phe Ser His Leu Ser Phe Ser Leu Ser Asp 215 220 225 Glu Gln Glu Asn Ser His Thr Leu Leu Ser His Asn Ala Cys Asn 230 235 240 Lys Leu Ser His Pro Met Val Ala Ile Pro Glu His Glu Ala Leu 245 250 255 Asp Ser Lys Glu Gln 260 52 364 PRT Homo sapiens misc_feature Incyte ID No 1737459CD1 52 Met Ser Ala Asn Ser Ser Arg Val Gly Gln Leu Leu Leu Gln Gly 1 5 10 15 Ser Ala Cys Ile Arg Trp Lys Gln Asp Val Glu Gly Ala Ile Tyr 20 25 30 His Leu Ala Asn Cys Leu Leu Leu Leu Gly Phe Met Gly Gly Ser 35 40 45 Gly Val Tyr Gly Cys Phe Tyr Leu Phe Gly Phe Leu Ser Ala Gly 50 55 60 Tyr Leu Cys Cys Val Leu Trp Gly Trp Phe Ser Ala Cys Gly Leu 65 70 75 Asp Ile Val Leu Trp Ser Phe Leu Leu Ala Val Val Cys Leu Leu 80 85 90 Gln Leu Ala His Leu Val Tyr Arg Leu Arg Glu Asp Thr Leu Pro 95 100 105 Glu Glu Phe Asp Leu Leu Tyr Lys Thr Leu Cys Leu Pro Leu Gln 110 115 120 Val Pro Leu Gln Thr Tyr Lys Glu Ile Val His Cys Cys Glu Glu 125 130 135 Gln Val Leu Thr Leu Ala Thr Glu Gln Thr Tyr Ala Val Glu Gly 140 145 150 Glu Thr Pro Ile Asn Arg Leu Ser Leu Leu Leu Ser Gly Arg Val 155 160 165 Arg Val Ser Gln Asp Gly Gln Phe Leu His Tyr Ile Phe Pro Tyr 170 175 180 Gln Phe Met Asp Ser Pro Glu Trp Glu Ser Leu Gln Pro Ser Glu 185 190 195 Glu Gly Val Phe Gln Val Thr Leu Thr Ala Glu Thr Ser Cys Ser 200 205 210 Tyr Ile Ser Trp Pro Arg Lys Ser Leu His Leu Leu Leu Thr Lys 215 220 225 Glu Arg Tyr Ile Ser Cys Leu Phe Ser Ala Leu Leu Gly Tyr Asp 230 235 240 Ile Ser Glu Lys Leu Tyr Thr Leu Asn Asp Lys Leu Phe Ala Lys 245 250 255 Phe Gly Leu Arg Phe Asp Ile Arg Leu Pro Ser Leu Tyr His Val 260 265 270 Leu Gly Pro Thr Ala Ala Asp Ala Gly Pro Glu Ser Glu Lys Gly 275 280 285 Asp Glu Glu Val Cys Glu Pro Ala Val Ser Pro Pro Gln Ala Thr 290 295 300 Pro Thr Ser Leu Gln Gln Thr Pro Pro Cys Ser Thr Pro Pro Ala 305 310 315 Thr Thr Asn Phe Pro Ala Pro Pro Thr Arg Ala Arg Leu Ser Arg 320 325 330 Pro Asp Ser Gly Ile Leu Ala Ser Arg Ile Pro Leu Gln Ser Tyr 335 340 345 Ser Gln Val Ile Ser Arg Gly Gln Ala Pro Leu Ala Pro Thr His 350 355 360 Thr Pro Glu Leu 53 527 PRT Homo sapiens misc_feature Incyte ID No 058201CD1 53 Met Glu Cys Leu Val Ala Asp Lys Gln Asn Phe His Lys Ser Cys 1 5 10 15 Phe Arg Cys His His Cys Asn Ser Lys Leu Ser Leu Gly Asn Tyr 20 25 30 Ala Ser Leu His Gly Gln Ile Tyr Cys Lys Pro His Phe Lys Gln 35 40 45 Leu Phe Lys Ser Lys Gly Asn Tyr Asp Glu Gly Phe Gly His Lys 50 55 60 Gln His Lys Asp Arg Trp Asn Cys Lys Asn Gln Ser Arg Ser Val 65 70 75 Asp Phe Ile Pro Asn Glu Glu Pro Asn Met Cys Lys Asn Ile Ala 80 85 90 Glu Asn Thr Leu Val Pro Gly Asp Arg Asn Glu His Leu Asp Ala 95 100 105 Gly Asn Ser Glu Gly Gln Arg Asn Asp Leu Arg Lys Leu Gly Glu 110 115 120 Arg Gly Lys Leu Lys Val Ile Trp Pro Pro Ser Lys Glu Ile Pro 125 130 135 Lys Lys Thr Leu Pro Phe Glu Glu Glu Leu Lys Met Ser Lys Pro 140 145 150 Lys Trp Pro Pro Glu Met Thr Thr Leu Leu Ser Pro Glu Phe Lys 155 160 165 Ser Glu Ser Leu Leu Glu Asp Val Arg Thr Pro Glu Asn Lys Gly 170 175 180 Gln Arg Gln Asp His Phe Pro Phe Leu Gln Pro Tyr Leu Gln Ser 185 190 195 Thr His Val Cys Gln Lys Glu Asp Val Ile Gly Ile Lys Glu Met 200 205 210 Lys Met Pro Glu Gly Arg Lys Asp Glu Lys Lys Glu Gly Arg Lys 215 220 225 Asn Val Gln Asp Arg Pro Ser Glu Ala Glu Asp Thr Lys Ser Asn 230 235 240 Arg Lys Ser Ala Met Asp Leu Asn Asp Asn Asn Asn Val Ile Val 245 250 255 Gln Ser Ala Glu Lys Glu Lys Asn Glu Lys Thr Asn Gln Thr Asn 260 265 270 Gly Ala Glu Val Leu Gln Val Thr Asn Thr Asp Asp Glu Met Met 275 280 285 Pro Glu Asn His Lys Glu Asn Leu Asn Lys Asn Asn Asn Asn Asn 290 295 300 Tyr Val Ala Val Ser Tyr Leu Asn Asn Cys Arg Gln Lys Thr Ser 305 310 315 Ile Leu Glu Phe Leu Asp Leu Leu Pro Leu Ser Ser Glu Ala Asn 320 325 330 Asp Thr Ala Asn Glu Tyr Glu Ile Glu Lys Leu Glu Asn Thr Ser 335 340 345 Arg Ile Ser Glu Leu Leu Gly Ile Phe Glu Ser Glu Lys Thr Tyr 350 355 360 Ser Arg Asn Val Leu Ala Met Ala Leu Lys Lys Gln Thr Asp Arg 365 370 375 Ala Ala Ala Gly Ser Pro Val Gln Pro Ala Pro Lys Pro Ser Leu 380 385 390 Ser Arg Gly Leu Met Val Lys Gly Gly Ser Ser Ile Ile Ser Pro 395 400 405 Asp Thr Asn Leu Leu Asn Ile Lys Gly Ser His Ser Lys Ser Lys 410 415 420 Asn Leu His Phe Phe Phe Ser Asn Thr Val Lys Ile Thr Ala Phe 425 430 435 Ser Lys Lys Asn Glu Asn Ile Phe Asn Cys Asp Leu Ile Asp Ser 440 445 450 Val Asp Gln Ile Lys Asn Met Pro Cys Leu Asp Leu Arg Glu Phe 455 460 465 Gly Lys Asp Val Lys Pro Trp His Val Glu Thr Thr Glu Ala Ala 470 475 480 Arg Asn Asn Glu Asn Thr Gly Phe Asp Ala Leu Ser His Glu Cys 485 490 495 Thr Ala Lys Pro Leu Phe Pro Arg Val Glu Val Gln Ser Glu Gln 500 505 510 Leu Thr Val Glu Glu Gln Ile Lys Arg Asn Arg Cys Tyr Ser Asp 515 520 525 Thr Glu 54 82 PRT Homo sapiens misc_feature Incyte ID No 5449893CD1 54 Met Ser Gln Ala Gly Ala Gln Glu Ala Pro Ile Lys Lys Lys Arg 1 5 10 15 Pro Pro Val Lys Glu Glu Asp Leu Lys Gly Ala Arg Gly Asn Leu 20 25 30 Thr Lys Asn Gln Glu Ile Lys Ser Lys Thr Tyr Gln Val Met Arg 35 40 45 Glu Cys Glu Gln Ala Gly Ser Ala Ala Pro Ser Val Phe Ser Arg 50 55 60 Thr Arg Thr Gly Thr Glu Thr Val Phe Glu Lys Pro Lys Ala Gly 65 70 75 Pro Thr Lys Ser Val Phe Gly 80 55 302 PRT Homo sapiens misc_feature Incyte ID No 282977CD1 55 Met Asn Val Gln Pro Cys Ser Arg Cys Gly Tyr Gly Val Tyr Pro 1 5 10 15 Ala Glu Lys Ile Ser Cys Ile Asp Gln Ile Trp His Lys Ala Cys 20 25 30 Phe His Cys Glu Val Cys Lys Met Met Leu Ser Val Asn Asn Phe 35 40 45 Val Ser His Gln Lys Lys Pro Tyr Cys His Ala His Asn Pro Lys 50 55 60 Asn Asn Thr Phe Thr Ser Val Tyr His Thr Pro Leu Asn Leu Asn 65 70 75 Val Arg Thr Phe Pro Glu Ala Ile Ser Gly Ile His Asp Gln Glu 80 85 90 Asp Gly Glu Gln Cys Lys Ser Val Phe His Trp Asp Met Lys Ser 95 100 105 Lys Asp Lys Glu Gly Ala Pro Asn Arg Gln Pro Leu Ala Asn Glu 110 115 120 Arg Ala Tyr Trp Thr Gly Tyr Gly Glu Gly Asn Ala Trp Cys Pro 125 130 135 Gly Ala Leu Pro Asp Pro Glu Ile Val Arg Met Val Glu Ala Arg 140 145 150 Lys Ser Leu Gly Glu Glu Tyr Thr Glu Asp Tyr Glu Gln Pro Arg 155 160 165 Gly Lys Gly Ser Phe Pro Ala Met Ile Thr Pro Ala Tyr Gln Arg 170 175 180 Ala Lys Lys Ala Asn Gln Leu Ala Ser Gln Val Glu Tyr Lys Arg 185 190 195 Gly His Asp Glu Arg Ile Ser Arg Phe Ser Thr Val Ala Asp Thr 200 205 210 Pro Glu Leu Leu Arg Ser Lys Ala Gly Ala Gln Leu Gln Ser Asp 215 220 225 Val Arg Tyr Thr Glu Asp Tyr Glu Gln Gln Arg Gly Lys Gly Ser 230 235 240 Phe Pro Ala Met Ile Thr Pro Ala Tyr Gln Ile Ala Lys Arg Ala 245 250 255 Asn Glu Leu Ala Ser Asp Val Arg Tyr His Gln Gln Tyr Gln Lys 260 265 270 Glu Met Arg Gly Met Ala Gly Pro Ala Ile Gly Ala Glu Gly Ile 275 280 285 Leu Thr Arg Glu Cys Ala Asp Gln Tyr Gly His Gly Tyr Pro Glu 290 295 300 Glu Tyr 56 193 PRT Homo sapiens misc_feature Incyte ID No 3178454CD1 56 Met Asn Thr Ser Phe Ser Asp Ile Glu Leu Leu Glu Asp Ser Gly 1 5 10 15 Ile Pro Thr Glu Ala Phe Leu Ala Ser Cys Cys Ala Val Val Pro 20 25 30 Val Leu Asp Lys Leu Gly Pro Thr Val Phe Ala Pro Val Lys Met 35 40 45 Asp Leu Val Glu Asn Ile Lys Lys Val Asn Gln Lys Tyr Ile Thr 50 55 60 Asn Lys Glu Glu Phe Thr Thr Leu Gln Lys Ile Val Leu His Glu 65 70 75 Val Glu Ala Asp Val Ala Gln Val Arg Asn Ser Ala Thr Glu Ala 80 85 90 Leu Leu Trp Leu Lys Arg Gly Leu Lys Phe Leu Lys Gly Phe Leu 95 100 105 Thr Glu Val Lys Asn Gly Glu Lys Asp Ile Gln Thr Ala Leu Asn 110 115 120 Asn Ala Tyr Gly Lys Thr Leu Arg Gln His His Gly Trp Val Val 125 130 135 Arg Gly Val Phe Ala Leu Ala Leu Arg Ala Thr Pro Ser Tyr Glu 140 145 150 Asp Phe Val Ala Ala Leu Thr Val Lys Glu Gly Asp His Arg Lys 155 160 165 Glu Ala Phe Ser Ile Gly Met Gln Arg Asp Leu Ser Leu Tyr Leu 170 175 180 Pro Ala Met Lys Lys Gln Met Ala Ile Leu Asp Ala Leu 185 190 57 174 PRT Homo sapiens misc_feature Incyte ID No 4152861CD1 57 Met Ser Asn Gly Tyr Arg Thr Leu Ser Gln His Leu Asn Asp Leu 1 5 10 15 Lys Lys Glu Asn Phe Ser Leu Lys Leu Arg Ile Tyr Phe Leu Glu 20 25 30 Glu Arg Met Gln Gln Lys Tyr Glu Ala Ser Arg Glu Asp Ile Tyr 35 40 45 Lys Arg Asn Thr Glu Leu Lys Val Glu Val Glu Ser Leu Lys Arg 50 55 60 Glu Leu Gln Asp Lys Lys Gln His Leu Asp Lys Thr Trp Ala Asp 65 70 75 Val Glu Asn Leu Asn Ser Gln Asn Glu Ala Glu Leu Arg Arg Gln 80 85 90 Phe Glu Glu Arg Gln Gln Glu Thr Glu His Val Tyr Glu Leu Leu 95 100 105 Glu Asn Lys Met Gln Leu Leu Gln Glu Glu Ser Arg Leu Ala Lys 110 115 120 Asn Glu Ala Ala Arg Met Ala Ala Leu Val Glu Ala Glu Lys Glu 125 130 135 Cys Asn Leu Glu Leu Ser Glu Lys Leu Lys Gly Val Thr Lys Asn 140 145 150 Trp Glu Asp Val Pro Gly Asp Gln Val Lys Pro Asp Gln Tyr Thr 155 160 165 Glu Ala Leu Ala Gln Arg Asp Lys Ile 170 58 230 PRT Homo sapiens misc_feature Incyte ID No 3009303CD1 58 Met Val Gly Val Arg Glu Pro Leu Val Phe Arg Val Asp Ala Arg 1 5 10 15 Gly Ser Val Asp Trp Ala Ala Ser Gly Met Gly Ser Leu Glu Glu 20 25 30 Glu Gly Thr Met Glu Glu Ala Gly Glu Glu Glu Gly Glu Asp Gly 35 40 45 Asp Ala Phe Val Thr Glu Glu Ser Gln Asp Thr His Ser Leu Gly 50 55 60 Asp Arg Asp Pro Lys Ile Leu Thr His Asn Gly Arg Met Leu Thr 65 70 75 Leu Ala Asp Leu Glu Asp Tyr Val Pro Gly Glu Gly Glu Thr Phe 80 85 90 His Cys Gly Gly Pro Gly Pro Gly Ala Pro Asp Asp Pro Pro Cys 95 100 105 Glu Val Ser Val Ile Gln Arg Glu Ile Gly Glu Pro Thr Val Gly 110 115 120 Gln Pro Val Leu Leu Ser Val Gly His Ala Leu Gly Pro Arg Gly 125 130 135 Pro Leu Gly Leu Phe Arg Pro Glu Pro Arg Gly Ala Ser Pro Pro 140 145 150 Gly Pro Gln Val Arg Ser Leu Glu Gly Thr Ser Phe Leu Leu Arg 155 160 165 Glu Ala Pro Ala Arg Pro Val Gly Ser Ala Pro Trp Thr Gln Ser 170 175 180 Phe Cys Thr Arg Ile Arg Arg Ser Ala Asp Ser Gly Gln Ser Ser 185 190 195 Phe Thr Thr Glu Leu Ser Thr Gln Thr Val Asn Phe Gly Thr Val 200 205 210 Gly Glu Thr Val Thr Leu His Ile Cys Pro Asp Arg Asp Gly Asp 215 220 225 Glu Ala Ala Gln Pro 230 59 915 PRT Homo sapiens misc_feature Incyte ID No 4151935CD1 59 Met Pro Leu Phe Glu Ala Glu Glu Gly Val Leu Ser Arg Thr Gln 1 5 10 15 Ile Phe Pro Thr Thr Ile Lys Val Ile Asp Pro Glu Phe Leu Glu 20 25 30 Glu Pro Pro Ala Leu Ala Phe Leu Tyr Lys Asp Leu Tyr Glu Glu 35 40 45 Ala Val Gly Glu Lys Lys Lys Glu Glu Glu Thr Ala Ser Glu Gly 50 55 60 Asp Ser Val Asn Ser Glu Ala Ser Phe Pro Ser Arg Asn Ser Asp 65 70 75 Thr Asp Asp Gly Thr Gly Ile Tyr Phe Glu Lys Tyr Ile Leu Lys 80 85 90 Asp Asp Ile Leu His Asp Thr Ser Leu Thr Gln Lys Asp Gln Gly 95 100 105 Gln Gly Leu Glu Glu Lys Arg Val Gly Lys Asp Asp Ser Tyr Gln 110 115 120 Pro Ile Ala Ala Glu Gly Glu Ile Trp Gly Lys Phe Gly Thr Ile 125 130 135 Cys Arg Glu Lys Ser Leu Glu Glu Gln Lys Gly Val Tyr Gly Glu 140 145 150 Gly Glu Ser Val Asp His Val Glu Thr Val Gly Asn Val Ala Met 155 160 165 Gln Lys Lys Ala Pro Ile Thr Glu Asp Val Arg Val Ala Thr Gln 170 175 180 Lys Ile Ser Tyr Ala Val Pro Phe Glu Asp Thr His His Val Leu 185 190 195 Glu Arg Ala Asp Glu Ala Gly Ser His Gly Asn Glu Val Gly Asn 200 205 210 Ala Ser Pro Glu Val Asn Leu Asn Val Pro Val Gln Val Ser Phe 215 220 225 Pro Glu Glu Glu Phe Ala Ser Gly Ala Thr His Val Gln Glu Thr 230 235 240 Ser Leu Glu Glu Pro Lys Ile Leu Val Pro Pro Glu Pro Ser Glu 245 250 255 Glu Arg Leu Arg Asn Ser Pro Val Gln Asp Glu Tyr Glu Phe Thr 260 265 270 Glu Ser Leu His Asn Glu Val Val Pro Gln Asp Ile Leu Ser Glu 275 280 285 Glu Leu Ser Ser Glu Ser Thr Pro Glu Asp Val Leu Ser Gln Gly 290 295 300 Lys Glu Ser Phe Glu His Ile Ser Glu Asn Glu Phe Ala Ser Glu 305 310 315 Ala Glu Gln Ser Thr Pro Ala Glu Gln Lys Glu Leu Gly Ser Glu 320 325 330 Arg Lys Glu Glu Asp Gln Leu Ser Ser Glu Val Val Thr Glu Lys 335 340 345 Ala Gln Lys Glu Leu Lys Lys Ser Gln Ile Asp Thr Tyr Cys Tyr 350 355 360 Thr Cys Lys Cys Pro Ile Ser Ala Thr Asp Lys Val Phe Gly Thr 365 370 375 His Lys Asp His Glu Val Ser Thr Leu Asp Thr Ala Ile Ser Ala 380 385 390 Val Lys Val Gln Leu Ala Glu Phe Leu Glu Asn Leu Gln Glu Lys 395 400 405 Ser Leu Arg Ile Glu Ala Phe Val Ser Glu Ile Glu Ser Phe Phe 410 415 420 Asn Thr Ile Glu Glu Asn Cys Ser Lys Asn Glu Lys Arg Leu Glu 425 430 435 Glu Gln Asn Glu Glu Met Met Lys Lys Val Leu Ala Gln Tyr Asp 440 445 450 Glu Lys Ala Gln Ser Phe Glu Glu Val Lys Lys Lys Lys Met Glu 455 460 465 Phe Leu His Glu Gln Met Val His Phe Leu Gln Ser Met Asp Thr 470 475 480 Ala Lys Asp Thr Leu Glu Thr Ile Val Arg Glu Ala Glu Glu Leu 485 490 495 Asp Glu Ala Val Phe Leu Thr Ser Phe Glu Glu Ile Asn Glu Arg 500 505 510 Leu Leu Ser Ala Met Glu Ser Thr Ala Ser Leu Glu Lys Met Pro 515 520 525 Ala Ala Phe Ser Leu Phe Glu His Tyr Asp Asp Ser Ser Ala Arg 530 535 540 Ser Asp Gln Met Leu Lys Gln Val Ala Val Pro Gln Pro Pro Arg 545 550 555 Leu Glu Pro Gln Glu Pro Asn Ser Ala Thr Ser Thr Thr Ile Ala 560 565 570 Val Tyr Trp Ser Met Asn Lys Glu Asp Val Ile Asp Ser Phe Gln 575 580 585 Val Tyr Cys Met Glu Glu Pro Gln Asp Asp Gln Glu Val Asn Glu 590 595 600 Leu Val Glu Glu Tyr Arg Leu Thr Val Lys Glu Ser Tyr Cys Ile 605 610 615 Phe Glu Asp Leu Glu Pro Asp Arg Cys Tyr Gln Val Trp Val Met 620 625 630 Ala Val Asn Phe Thr Gly Cys Ser Leu Pro Ser Glu Arg Ala Ile 635 640 645 Phe Arg Thr Ala Pro Ser Thr Pro Val Ile Arg Ala Glu Asp Cys 650 655 660 Thr Val Cys Trp Asn Thr Ala Thr Ile Arg Trp Arg Pro Thr Thr 665 670 675 Pro Glu Ala Thr Glu Thr Tyr Thr Leu Glu Tyr Cys Arg Gln His 680 685 690 Ser Pro Glu Gly Glu Gly Leu Arg Ser Phe Ser Gly Ile Lys Gly 695 700 705 Leu Gln Leu Lys Val Asn Leu Gln Pro Asn Asp Asn Tyr Phe Phe 710 715 720 Tyr Val Arg Ala Ile Asn Ala Phe Gly Thr Ser Glu Gln Ser Glu 725 730 735 Ala Ala Leu Ile Ser Thr Arg Gly Thr Arg Phe Leu Leu Leu Arg 740 745 750 Glu Thr Ala His Pro Ala Leu His Ile Ser Ser Ser Gly Thr Val 755 760 765 Ile Ser Phe Gly Glu Arg Arg Arg Leu Thr Glu Ile Pro Ser Val 770 775 780 Leu Gly Glu Glu Leu Pro Ser Cys Gly Gln His Tyr Trp Glu Thr 785 790 795 Thr Val Thr Asp Cys Pro Ala Tyr Arg Leu Gly Ile Cys Ser Ser 800 805 810 Ser Ala Val Gln Ala Gly Ala Leu Gly Gln Gly Glu Thr Ser Trp 815 820 825 Tyr Met His Cys Ser Glu Pro Gln Arg Tyr Thr Phe Phe Tyr Ser 830 835 840 Gly Ile Val Ser Asp Val His Val Thr Glu Arg Pro Ala Arg Val 845 850 855 Gly Ile Leu Leu Asp Tyr Asn Asn Gln Arg Leu Ile Phe Ile Asn 860 865 870 Ala Glu Ser Glu Gln Leu Leu Phe Ile Ile Arg His Arg Phe Asn 875 880 885 Glu Gly Val His Pro Ala Phe Ala Leu Glu Lys Pro Gly Lys Cys 890 895 900 Thr Leu His Leu Gly Ile Glu Pro Pro Asp Ser Val Arg His Lys 905 910 915 60 163 PRT Homo sapiens misc_feature Incyte ID No 3012947CD1 60 Met Ala Leu Glu Gln Lys Glu Leu Asp Gln Glu Pro Gly Ala Gly 1 5 10 15 Leu Asp Ser Leu Ile Arg Thr Gly Ser Ser Cys Gln Asn Pro Gly 20 25 30 Cys Asp Ala Val Tyr Gln Gly Pro Glu Ser Asp Ala Thr Pro Cys 35 40 45 Thr Tyr His Pro Gly Ala Pro Arg Phe His Glu Gly Met Lys Ser 50 55 60 Trp Ser Cys Cys Gly Ile Gln Thr Leu Asp Phe Gly Ala Phe Leu 65 70 75 Ala Gln Pro Gly Cys Arg Val Gly Arg His Asp Trp Gly Lys Gln 80 85 90 Leu Pro Ala Ser Cys Arg His Asp Trp His Gln Thr Asp Ser Leu 95 100 105 Val Val Val Thr Val Tyr Gly Gln Ile Pro Leu Pro Ala Phe Asn 110 115 120 Trp Val Lys Ala Ser Gln Thr Glu Leu His Val His Ile Val Phe 125 130 135 Asp Gly Asn Arg Val Phe Gln Ala Gln Met Lys Leu Trp Gly Val 140 145 150 Ser Glu Asp Gln Gly Thr Gln Glu Trp Glu Ala Asp Gly 155 160 61 201 PRT Homo sapiens misc_feature Incyte ID No 3009806CD1 61 Met Glu Asn Val Glu Val Phe Thr Ala Glu Gly Lys Gly Arg Gly 1 5 10 15 Leu Lys Ala Thr Lys Glu Phe Trp Ala Ala Asp Ile Ile Phe Ala 20 25 30 Glu Arg Ala Tyr Ser Ala Val Val Phe Asp Ser Leu Val Asn Phe 35 40 45 Val Cys His Thr Cys Phe Lys Arg Gln Glu Lys Leu His Arg Cys 50 55 60 Gly Gln Cys Lys Phe Ala His Tyr Cys Asp Arg Thr Cys Gln Lys 65 70 75 Asp Ala Trp Leu Asn His Lys Asn Glu Cys Ser Ala Ile Lys Arg 80 85 90 Tyr Gly Lys Val Pro Asn Glu Asn Ile Arg Leu Ala Ala Arg Ile 95 100 105 Met Trp Arg Val Glu Arg Glu Gly Thr Gly Leu Thr Glu Gly Cys 110 115 120 Leu Val Ser Val Asp Asp Leu Gln Asn His Val Glu His Phe Gly 125 130 135 Glu Glu Glu Gln Lys Asp Leu Arg Val Asp Val Asp Thr Phe Leu 140 145 150 Gln Tyr Trp Pro Ala Gln Ser Gln Gln Phe Ser Met Gln Tyr Ile 155 160 165 Ser His Ile Phe Gly Val Ile Asn Cys Asn Gly Phe Thr Leu Ser 170 175 180 Asp Gln Arg Gly Leu His Ser Val Gly Arg Lys Asp Leu Ser Pro 185 190 195 Pro Gly Ala Gly Glu Pro 200 62 329 PRT Homo sapiens misc_feature Incyte ID No 5578191CD1 62 Met Glu Asp Ser Glu Ala Val Gln Arg Ala Thr Ala Leu Ile Glu 1 5 10 15 Gln Arg Leu Ala Gln Glu Glu Glu Asn Glu Lys Leu Arg Gly Asp 20 25 30 Thr Arg Gln Lys Leu Pro Met Asp Leu Leu Val Leu Glu Asp Glu 35 40 45 Lys His His Gly Ala Gln Ser Ala Ala Leu Gln Lys Val Lys Gly 50 55 60 Gln Glu Arg Val Arg Lys Thr Ser Leu Asp Leu Arg Arg Glu Ile 65 70 75 Ile Asp Val Gly Gly Ile Gln Asn Leu Ile Glu Leu Arg Lys Lys 80 85 90 Arg Lys Gln Lys Lys Arg Asp Ala Leu Ala Ala Ser His Glu Pro 95 100 105 Pro Pro Glu Pro Glu Glu Ile Thr Gly Pro Val Asp Glu Glu Thr 110 115 120 Phe Leu Lys Ala Ala Val Glu Gly Lys Met Lys Val Ile Glu Lys 125 130 135 Phe Leu Ala Asp Gly Gly Ser Ala Asp Thr Cys Asp Gln Phe Arg 140 145 150 Arg Thr Ala Leu His Arg Ala Ser Leu Glu Gly His Met Glu Ile 155 160 165 Leu Glu Lys Leu Leu Asp Asn Gly Ala Thr Val Asp Phe Gln Asp 170 175 180 Arg Leu Asp Cys Thr Ala Met His Trp Ala Cys Arg Gly Gly His 185 190 195 Leu Glu Val Val Lys Leu Leu Gln Ser His Gly Ala Asp Thr Asn 200 205 210 Val Arg Asp Lys Leu Leu Ser Thr Pro Leu His Val Ala Val Arg 215 220 225 Thr Gly Gln Val Glu Ile Val Glu His Phe Leu Ser Leu Gly Leu 230 235 240 Glu Ile Asn Ala Arg Asp Arg Glu Gly Asp Thr Ala Leu His Asp 245 250 255 Ala Val Arg Leu Asn Arg Tyr Lys Ile Ile Lys Leu Leu Leu Leu 260 265 270 His Gly Ala Asp Met Met Thr Lys Asn Leu Ala Gly Lys Thr Pro 275 280 285 Thr Asp Leu Val Gln Leu Trp Gln Ala Asp Thr Arg His Ala Leu 290 295 300 Glu His Pro Glu Pro Gly Ala Glu His Asn Gly Leu Glu Gly Pro 305 310 315 Asn Asp Ser Gly Arg Glu Thr Pro Gln Pro Val Pro Ala Gln 320 325 

What is claimed is:
 1. A composition comprising a plurality of polynucleotides having the nucleic acid sequences of SEQ ID NOs:1-48 or the complements thereof.
 2. An isolated polynucleotide comprising a nucleic acid sequence selected from SEQ ID NOs:1-48 and the complements thereof.
 3. A composition comprising a polynucleotide of claim 2 and a labeling moiety.
 4. A method of using a polynucleotide to screen a plurality of molecules to identify at least one ligand which specifically binds the polynucleotide, the method comprising: a) combining the composition of claim 1 with a plurality of molecules under conditions to allow specific binding; and b) detecting specific binding, thereby identifying a ligand which specifically binds a polynucleotide.
 5. The method of claim 4 wherein the composition is attached to a substrate.
 6. The method of claim 4 wherein the molecules to be screened are selected from DNA molecules, RNA molecules, peptide nucleic acids, mimetics, and proteins.
 7. A method of using a polynucleotide to purify a ligand, the method comprising: a) combining the polynucleotide of claim 2 with a sample under conditions to allow specific binding; b) recovering the bound polynucleotide; and c) separating the ligand from the bound polynucleotide, thereby obtaining purified ligand.
 8. The method of claim 7 wherein the polynucleotide is attached to a substrate.
 9. A method for using a polynucleotide to detect gene expression in a sample, the method comprising: a) hybridizing the composition of claim 1 to a sample thereby forming at least one hybridization complex; b) detecting complex formation, wherein complex formation indicates gene expression in the sample.
 10. The method of claim 9 wherein the polynucleotides of the composition are attached to a substrate.
 11. The method of claim 9 wherein the sample is from pancreatic tissue.
 12. The method of claim 9 wherein gene expression is compared to standards and indicates the presence of type I diabetes.
 13. A vector comprising a polynucleotide of claim
 2. 14. A host cell comprising the vector of claim
 13. 15. A method for using a host cell to produce a protein, the method comprising: a) culturing the host cell of claim 14 under conditions for expression of the protein; and b) recovering the protein from cell culture.
 16. A purified protein or a portion thereof comprising an amino acid sequence selected from SEQ ID NO:49-62.
 17. A composition comprising the protein of claim 16 and a pharmaceutical carrier or a labeling moiety.
 18. A method for using a protein to screen a plurality of molecules to identify at least one ligand which specifically binds the protein, the method comprising: a) combining the protein of claim 16 with the plurality of molecules under conditions to allow specific binding; and b) detecting specific binding between the protein and ligand, thereby identifying a ligand which specifically binds the polypeptide.
 19. The method of claim 18 wherein the plurality of molecules is selected from DNA molecules, RNA molecules, peptide nucleic acids, mimetics, proteins, agonists, antagonists, and antibodies.
 20. A method of using a protein to prepare and purify antibodies comprising: a) immunizing a animal with the protein of claim 16 under conditions to elicit an antibody response; b) isolating animal antibodies; c) attaching the protein to a substrate; d) contacting the substrate with isolated antibodies under conditions to allow specific binding to the protein; e) dissociating the antibodies from the protein, thereby obtaining purified antibodies. 